Updated 10 hours ago · U.S. FDA & CPSC

Recalls today

Every new U.S. recall of food, medicines, medical devices and household products, in one place, updated every day. Search for a product or brand you own.

Counts are for the last 30 days.

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Latest recalls

Food · Oct 14, 2026 · Class I · Ongoing

BiQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA COLOMBIANA

A&P CREATIONS · Clermont, FL, United States

Why: Product contains undeclared Sildenafil and Tadalafil.

Product details, where it was sold and what to do

biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA COLOMBIANA; Distributed by: Biofel

Quantity: 3,116 bottles

Distribution: Distributed nationwide (US).

Recall number H-0017-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

Saint Francis Apizza Frozen Supreme Pizza, Net Weight: 17 oz

Saint Francis Apizza LLC · Cincinnati, OH, United States

Why: Undeclared soy allergen: soybean oil and soy lecithin

Product details, where it was sold and what to do

Saint Francis Apizza Frozen Supreme Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27760 7

Quantity: 1,920 individual units

Distribution: KY, OH

Recall number H-0024-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class I · Ongoing

Berlin Seeds Alfalfa Sprouting Seeds, packaged in 1/4 lb., 1/2 lb., 1 lb., and 5 lb

Berlin Seeds · Millersburg, OH, United States

Why: Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination.

Product details, where it was sold and what to do

Berlin Seeds Alfalfa Sprouting Seeds, packaged in 1/4 lb., 1/2 lb., 1 lb., and 5 lb. resealable bags and 50 lb. woven poly bags

Quantity: 950 lbs.

Distribution: Through the firm's retail store in Millersburg, OH and nationwide through the firm's website

Recall number H-0013-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class I · Ongoing

Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case

The Better Bakehouse Snack Company · Las Vegas, NV, United States

Why: Undeclared Milk.

Product details, where it was sold and what to do

Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC 850041392103. Paperboard carton containing 5 individually wrapped packages of two donuts each. UPC: 850041392103. The Better Bakehouse Snack Co. 3651 Lindell Rd, Suite D700 Las Vegas, NV 89103

Quantity: 10,602 consumer units

Distribution: Product was distributed nationwide.

Recall number H-0011-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class I · Ongoing

Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering

GIAS FOOD INC. · New York, NY, United States

Why: Contamination with Listeria monocytogenes

Product details, where it was sold and what to do

Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 PRODUCT OF ITALY

Quantity: 1174 cases

Distribution: Retail locations nationwide

Recall number H-0014-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L

G L Mezzetta Inc · American Canyon, CA, United States

Why: Potential contamination with foreign objects: mice.

Product details, where it was sold and what to do

Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503 PRODUCT OF GREECE UPC: 073214003280

Quantity: 7,497 cases (6 units/case)

Distribution: Domestic: AZ, CA, CO, GA, IA, ID, IL, IN, MI, MN, MO, NC, OH, OK, OR, PA, SD, TX, UT, VA, WA, WI. Foreign: Not applicable.

Recall number H-0007-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz

Saint Francis Apizza LLC · Cincinnati, OH, United States

Why: Undeclared soy allergen: soybean oil and soy lecithin

Product details, where it was sold and what to do

Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27759 1

Quantity: 4,255 individual units

Distribution: KY, OH

Recall number H-0022-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

Croissant

J K Patisserie & Bakery LLC · Long Island City, NY, United States

Why: Egg was not declared in the Contains statement.

Product details, where it was sold and what to do

Croissant; packaged in cardboard box; Ingredients: King Midas Special (Wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid, malted barley flour), Veribest Pastry flour (Wheat Flour), Unsalted Butter, Milk, Water, Granulated Sugar, Yeast, Salt, eggs; Contains: Wheat, Milk

Quantity: 1,928 units

Distribution: NY and NJ

Recall number H-0027-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Completed

WinCo Foods Salsa Bean Dip Express Tray is packaged in a foil bottom container with clear plastic lid

WinCo Foods LLC · Boise, ID, United States

Why: Bean Dip Trays contains recalled Peperoncini (pepper) which was recalled due to pest issue.

Product details, where it was sold and what to do

WinCo Foods Salsa Bean Dip Express Tray is packaged in a foil bottom container with clear plastic lid. Net Wt. 54oz. UPC 2 67173 510983. WinCo Foods Salsa Bean Dip Tray 16inch (sold by catering special order only) is packaged in plastic tray container with clear plastic dome lid. Net Wt. 104oz. UPC 2 67240 ######. Both products sold refrigerated with a shelf life of 4 days from package date. Distributed by WinCo Foods 650 N. Armstrong Place Boise, ID.

Quantity: Salsa Bean Dip Express 54oz. trays (4266 units); Salsa Bean Dip 16inch Catering Tray (97 units).

Distribution: Distributed in AZ, CA, ID, MT, NV, OR, UT, and WA.

Recall number H-0008-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class I · Ongoing

LEASA Alfalfa Sprouts

LEASA Industries Co., Inc. · Miami, FL, United States

Why: Seeds may have been contaminated with E.coli

Product details, where it was sold and what to do

LEASA Alfalfa Sprouts; packaged in plastic clamshell containers; KEEP REFRIGERATED; NET WT. 6 OZ. (170g); Grown & Packaged by: LEASA Industries Co., Inc., Mami FL 33147; Product of USA; UPC: 0 75465 11111 0

Quantity: 1,416 cups

Distribution: FL and NH

Recall number H-0003-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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Food · Oct 14, 2026 · Class I · Ongoing

X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box

A&P CREATIONS · Clermont, FL, United States

Why: Product contains undeclared Sildenafil and Tadalafil.

Product details, where it was sold and what to do

X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.

Quantity: 1,283 retail units

Distribution: Distributed nationwide (US).

Recall number H-0016-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

Chocolate Chip Cookies packaged in a cardboard box

J K Patisserie & Bakery LLC · Long Island City, NY, United States

Why: Soy was not declared in the Contains statement.

Product details, where it was sold and what to do

Chocolate Chip Cookies packaged in a cardboard box; Ingredients: King Midas Special (Wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid, malted barley flour), Dark Chocolate Chip (sugar, unsweetened chocolate, cocoa butter, soy lecithin, ground vanilla beans), Unsalted Butter, Dark Brown Sugar, Wheat flour, Eggs, Salt, Baking Powder, Baking Soda, Veribest Pastry flour (Wheat Flour); Contains: Milk, Wheat, Eggs; JK Patisserie & Bakery LLC DBA Le Petit Paris

Quantity: 610 units

Distribution: NY and NJ

Recall number H-0026-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

Saint Francis Apizza Frozen Pepperoni Pizza, Net Weight: 17 oz

Saint Francis Apizza LLC · Cincinnati, OH, United States

Why: Undeclared soy allergen: soybean oil and soy lecithin

Product details, where it was sold and what to do

Saint Francis Apizza Frozen Pepperoni Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27762 1

Quantity: 4,931 individual units

Distribution: KY, OH

Recall number H-0021-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 14, 2026 · Class II · Ongoing

QUESO PALMITA

QUESO PALMITA GP LLC · Stafford, TX, United States

Why: Undeclared milk, cheese declared

Product details, where it was sold and what to do

QUESO PALMITA. Generic Name: Pastel de Queso (Cheese Pie). Intended use: Human consumption. Condition: Frozen. Shelf life or expected life: 90 days. Type of packaging: Vacuum, resealable package. Net weight: 1.2 lbs. UPC: 094922980045.

Quantity: 20 packages

Distribution: Texas

Recall number H-0015-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Consumer products · Oct 8, 2026

The Conqueror Recalls Avengers Medals Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets

Actionary Limited, dba The Conqueror, of New Zealand · China

Why: The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Product details, where it was sold and what to do

Avengers Infinity Gauntlet Medals. This recall involves the Avengers Infinity Gauntlet medal. The medal is gold, with colorful gems on the front and comes in a black package marked "Marvel Avengers" with Marvel Avengers artwork. The medals are part of the Avengers virtual challenge series. To receive the medal, customers must have completed the Infinity Gauntlet virtual challenge on the Conqueror App.

Quantity: About 476

Distribution: Sold at Sold Online At: www.theconqueror.events and through The Conqueror App from March 2026 through May 2026 for about $50.

Remedy: Consumers should stop using the Avengers Infinity Gauntlet Medal immediately and contact The Conqueror for instructions on receiving a full refund or a replacement medal. Consumers will be asked to cut the ribbon from the medal and write "RECALLED" in permanent marker on the medal and ribbon, throw the product away and email a photo of the disposed medal and ribbon to support@theconqueror.events.

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks Due to Risk of Serious Injury or Death from Burn and Fire Hazards

Snow Peak USA, Inc., of Portland, Oregon · China, Taiwan

Why: The fireplace's lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards.

Product details, where it was sold and what to do

Snow Peak Takibi Fireplace Propane Inserts and Lava Rocks. This recall involves the Takibi propane inserts and lava rocks, fireplace accessories that allows Snow Peak's Pack & Carry Fireplace L (ST-032) and XL (ST-034) to operate on propane fuel instead of wood or charcoal. The propane insert includes a detachable hose with a gas flow regulator that controls the intensity of the flame with the twist of a knob. The product also includes lava rocks. Model number ST-332-US can be found on the product packaging and in the user manual.

Quantity: About 100

Distribution: Sold at Sold Online At: Snowpeak.com from July 2026 through July 2026 for about $350.

Remedy: Consumers should stop using the propane insert and lava rocks fireplace accessories immediately and contact Snow Peak for a full refund. Consumers will be provided with a prepaid shipping label to return the propane insert and lava rocks. For replacement lava rocks only, the consumer can keep the propane inserts, and the firm will ship replacement lava rocks to the consumer. Do not use inserts unt

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

Romorgniz Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units

Zhangzhou Jinhao Sen Smart Home Co., Ltd., of China · China

Why: The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the  STURDY Act.

Product details, where it was sold and what to do

Romorgniz Six-Drawer Dressers. This recall involves Romorgniz six-drawer dressers. The wooden dressers were sold in white and black, measure about 27.6 inches wide, 15.6 inches long, 43.2 inches tall and weigh 73.3 pounds.

Quantity: About 12,078

Distribution: Sold at Sold Online At: Amazon.com from May 2025 through August 2026 for between $100 and $170.

Remedy: Consumers should stop using the recalled dressers immediately if they are not anchored to the wall, place them in an area that children cannot access and contact Romorgniz for a full refund. Consumers will be asked to write in permanent marker "RECALLED" on the top, front and sides of the dresser, remove all drawers and send photos of the marked and disassembled dresser to Romorgnizrecall@outlook.

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

Pacearth Direct Recalls PACEARTH Swing Seats Due to Risk of Serious Injury from Fall Hazard

Pacearth Direct, of City of Industry, California · China

Why: The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall hazard.

Product details, where it was sold and what to do

PACEARTH Swing Seats. This recall involves PACEARTH U-type swing seats. The swing seats were sold in various colors including green, blue, pink, red and turquoise. The chain is coated in yellow plastic. Metal carabiners or quick links and yellow webbing straps were included with the swing seats to attach the swing to outdoor swing sets or tree branches. The swing seats were sold as a single unit or a pack of two.

Quantity: About 110,550

Distribution: Sold at Sold Online At: Amazon.com from May 2017 through June 2026 for between $27 and $57.

Remedy: Consumers should stop using the recalled swing seats immediately and contact Pacearth Direct for a full refund. Consumers will be asked to write "RECALLED" on the swing seat with permanent marker, take a photo of it, including the PACEARTH logo and email to recall@pacearth.com.

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

ONTHEWEI Recalls Baby Bath Seats Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats

Hubei Youhong Trading Co., Ltd., dba ONTHEWEI, of China · China

Why: The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.

Product details, where it was sold and what to do

ONTHEWEI Baby Bath Seats. This recall involves ONTHEWEI-branded baby bath seats. They are sold in gray, pink, blue and mist green and have detachable restraint arms and suction cups on the underside. "Model No: MY002" and "Date of manufacturer: 2026/1/10" are printed on a label on the back of the bath seat.

Quantity: About 2,140

Distribution: Sold at Sold Online At: Amazon.com in April 2026 for between $40 and $50.

Remedy: Consumers should stop using the recalled bath seats immediately and contact ONTHEWEI for a full refund. Consumers will be asked to destroy the bath seat by writing in permanent marker "RECALLED" on the front of the bath seat, disassembling it by removing the back rest and arm restraints and cutting the three suction cups on the seat's underside and send a photo of the destroyed bath seat showing t

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

Giant Bicycle Recalls LED-Light Keys Included with SureLock Bike Lock Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries

Giant Bicycle, Inc., of Newbury Park, California · China

Why: The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard.  Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the inges…

Product details, where it was sold and what to do

LED-light bike lock keys. This recall involves Giant Bicycle-branded black-and-white LED-light bike lock keys that were included as part of a pre-keyed SureLock bicycle lock set that includes a bike lock and two-or-four keys without an LED-light (depending on the model). Only LED-light bike lock keys manufactured after March 2023 are included in this recall. The list of affected serial numbers is included in the table below. Serial numbers are located on the underside of the bike lock, as shown in the last picture above. Name Serial number From To SURELOCK PROTECTOR 1 DT 00000 2303 00000 2607 SURELOCK PROTECTOR 1 STD 00001 2303 00001 2607 SURELOCK PROTECTOR 1 LS 00002 2303 00002 2607 SURELOCK FLEX KEY COIL 15 00010 2303 00010 2607 SURELOCK FLEX KEY COIL 12 00011 2303 00011 2607 SURELOCK FLEX KEY 15 00013 2303 00013 2607 SURELOCK FLEX KEY 12 00014 2303 00014 2607 GIANT SURELOCK FLEX KEY COIL 12 00065 2303 00065 2607 GIANT SURELOCK FLEX KEY COIL 15 00066 2303 00066 2607

Quantity: About 3,630 (In addition, 1,395 in Canada)

Distribution: Sold at Sold At: Giant Bicycle authorized stores nationwide and online at https://www.giant-bicycles.com/us from March 2023 through August 2026 for between $25 and $65.

Remedy: Consumers should stop using the recalled LED-light key that was included with certain SureLock Bicycle Lock sets immediately and contact Giant Bicycle for a $5 refund. Consumers will be asked to bring the LED key to an authorized Giant retailer to participate in the recall and receive the refund. When returning the LED-light key to a retailer, consumers will be required to bring either the complet

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards

Generac Power Systems Inc., of Waukesha, Wisconsin · United State, Vietnam

Why: Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards.

Product details, where it was sold and what to do

DR Power Equipment Pilot and Premier Trimmer Mowers. This recall involves DR Power Equipment Pilot and Premier walk-behind trimmer mowers. The trimmer mowers are orange and black and have the DR Power logo on the top of the motor and on the top of the frame above the cutter head. The trimmer mowers are labeled "Premier" or "Pro" on the side of the frame. The model numbers are printed on a label located on the side of the product's frame. Recalled model numbers and product description, which include all serial numbers, are listed below. Model Number Product Description Serial Number Range T4X1076DMN DR TRIMMER PILOT 7.6 FPT DR MS All T4X1076DMNR DR TRIMMER PILOT 7.6 FPT DR MS RECON All T4X1076DMNSD DR TRIMMER PILOT 7.6 FPT DR MS SD All T4X1176DMN DR TRIMMER PILOT 7.6 FPT DR MS All T4X1176DMN-1 DR TRIMMER PILOT 7.6 FPT DR MS All T4X1176DMNR DR TRIMMER PILOT 7.6 FPT DR MS RECON All TR43076DMN DR TRIMMER PREMIER 7.6 FPT DR MS All TR43076DMNR DR TRIMMER PREMIER 7.6 FPT DR MS RECON All

Quantity: About 42,860 (In addition, about 340 were sold in Canada)

Distribution: Sold at Sold At: Ace, TSC, Bomgaars, other home improvement, hardware and independent power equipment stores nationwide and online at drpower.com from November 2022 through July 2026 for between $380 to $550.

Remedy: Consumers should stop using the recalled trimmer mowers immediately and contact DR Power Equipment for a free repair kit. If consumers have concerns about installing the repair kit, contact DR Power Equipment to schedule a free repair installation from an authorized dealer.

Official CPSC recall notice ↗

Consumer products · Oct 8, 2026

Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard

Decathlon America LLC, of San Francisco, California · China

Why: The recalled bicycles' front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard.

Product details, where it was sold and what to do

Van Rysel GRVL AF Bicycles. This recall involves adult multi-terrain gravel bicycles Van Rysel GRVL AF Sword Brown CN FR (model number 8911304), Van Rysel GRVL AF Apex Beige CN FR (model number 8911305), Van Rysel GRVL AF Sword Pink CN FR (model number 8911308), and Van Rysel GRVL AF GRX Black (model number 8929130). The recalled models were sold in sizes x-small, small, medium, large and x-large. The bicycles are designed for off-road gravel riding, road cycling, commuting and bikepacking. Each bicycle can be identified by the model name and Van Rysel Product ID located on the barcode sticker on the frame near the bottom bracket. Only Van Rysel bicycles with the following Product IDs/ SKUs are included in this recall. Product ID Model Name REI SKU REI Product Name 5476620 USA GRVL AF GRX Black CN FR 2464430001 GRVL AF 2 GRX, GRAPHITE BLACK 5476621 USA GRVL AF GRX Black CN FR 2464430002 GRVL AF 2 GRX, GRAPHITE BLACK 5476622 USA GRVL AF GRX Black CN FR 2464430003 GRVL AF 2 GRX, GRAPHITE BLACK 5476623 USA GRVL AF GRX Black CN FR 2464430004 5476624 USA GRVL AF GRX Black CN FR 2464430005 GRVL AF 2 GRX, GRAPHITE BLACK 5327224 USA GRVL AF Apex Beige CN FR 2464440001 GRVL AF 2 Apex, CREAM BEIGE 5327225 USA GRVL AF Apex Beige CN FR 2464440002 GRVL AF 2 Apex, CREAM BEIGE 5327226 USA GRVL AF Apex Beige CN FR 2464440003 GRVL AF 2 Apex, CREAM BEIGE 5327227 USA GRVL AF Apex Beige CN FR 2464440004 GRVL AF 2 Apex, CREAM BEIGE 5327228 USA GRVL AF Apex Beige CN FR 2464440005 GRVL AF 2 Apex, …

Quantity: About 1,150

Distribution: Sold at Sold At: REI Co-op stores nationwide and online at REI.com from March 2025 through August 2026 for between $1,400 and $2,300.

Remedy: Consumers should stop using the recalled bicycles immediately and take them to the nearest Recreational Equipment (REI Co-op) location for a free inspection and repair service of the front fork assembly. Anyone unable to visit an REI Co-op location can contact Decathlon Customer Service directly for assistance. Recalled models can be identified by the Van Rysel Product ID on the top right of the p

Official CPSC recall notice ↗

Medical devices · Oct 7, 2026 · Class II · Ongoing

SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, and SmartPath to Ingenia Elition X

Philips North America · Cambridge, MA, United States

Why: When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.

Product details, where it was sold and what to do

SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T, SmartPath to dStream for XR and 3.0T, and SmartPath to Ingenia Elition X; Model number (REF): 1. 781260 (1.5T), 2. 782112 (1.5T), 3. 782146 (1.5T), 4. 782165 (1.5T), 5. 782145 (3.0T), 6. 782164 (3.0T), 7. 781270 (XR and 3.0T), 8. 782113 (XR and 3.0T), 9. 782129 (XR and 3.0T), 10. 782118 (Ingenia Elition X), 11. 782144 (Ingenia Elition X), 12. 782163 (Ingenia Elition X); Software Versions: R11, R12 and R13;

Quantity: 200

Distribution: Worldwide distribution - Nationwide and the countries of Algeria, Argentina, Australia, Austria, Bangladesh, Belgium, Brazil, Canada, Chile, China, Colombia, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Equator. Guinea, Finland, France, French Guiana, Georgia, Germany, Ghana, Greece, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kyrgyzstan, Latvia, Lebanon, Luxembourg, Malaysia, Malta, Martinique, Mauritius, Mexico, Moldova, Monaco, Morocco, Myanmar, Namibia, Nepal, Netherlands, New Zealand, Nicaragua, …

Recall number Z-3314-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visual…

Karl Storz Endoscopy · El Segundo, CA, United States

Why: Due to incorrect inside packaging label for eyepiece.

Product details, where it was sold and what to do

HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.

Quantity: 6 eyepieces

Distribution: U.S. Nationwide distribution in the states of AZ, CA and MO.

Recall number Z-3333-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-Line, Yellow Model/Catalog Number: ASP-564008 Software Version: …

ASP Global, LLC. · Austell, GA, United States

Why: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

Product details, where it was sold and what to do

Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-Line, Yellow Model/Catalog Number: ASP-564008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No

Quantity: 15580

Distribution: US Nationwide distribution in the states of MO, NV, IN, MN, GA, WI, PA, TX, CT, LA, NJ, FL, AL, NY, SC, NE, NC, OH, AZ, CO, MA, IL, KY, CA, VA, ME, KS, MD, TN, MS, AR, WA, NM, MI, WY.

Recall number Z-0041-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 1 LINE (10) Model/Catalog Number: DT-7115-01Q Software Version: Not Applicable …

ASP Global, LLC. · Austell, GA, United States

Why: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

Product details, where it was sold and what to do

Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 1 LINE (10) Model/Catalog Number: DT-7115-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No

Quantity: 100

Distribution: US Nationwide distribution in the states of MO, NV, IN, MN, GA, WI, PA, TX, CT, LA, NJ, FL, AL, NY, SC, NE, NC, OH, AZ, CO, MA, IL, KY, CA, VA, ME, KS, MD, TN, MS, AR, WA, NM, MI, WY.

Recall number Z-0064-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12" X 3.5" 1-LINE (CS 12) PLUM Model/Catalog Number: A70107002 Software V…

ASP Global, LLC. · Austell, GA, United States

Why: Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

Product details, where it was sold and what to do

Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 12" X 3.5" 1-LINE (CS 12) PLUM Model/Catalog Number: A70107002 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No

Quantity: 1692

Distribution: US Nationwide distribution in the states of MO, NV, IN, MN, GA, WI, PA, TX, CT, LA, NJ, FL, AL, NY, SC, NE, NC, OH, AZ, CO, MA, IL, KY, CA, VA, ME, KS, MD, TN, MS, AR, WA, NM, MI, WY.

Recall number Z-0023-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

NOxBOXi Nitric Oxide Delivery System

NOXBOX LTD · Sittingbourne, United Kingdom

Why: Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.

Product details, where it was sold and what to do

NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.

Quantity: 1,667 units

Distribution: US Nationwide distribution in the state of Georgia.

Recall number Z-3306-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

PALACOS R pro 40; PALACOS R pro 80. Model/Catalog Numbers: 5081286; 5081287. Radiopaque, poly (methyl methacrylate)-based (PMMA) bone cemen…

Heraeus Medical GmbH (Dental Division) · Wehrheim, Germany

Why: Potential for monomer liquid leakage.

Product details, where it was sold and what to do

PALACOS R pro 40; PALACOS R pro 80. Model/Catalog Numbers: 5081286; 5081287. Radiopaque, poly (methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix).

Quantity: 33,727 units

Distribution: Worldwide distribution - US Nationwide and the countries of Aland Islands, Australia, Austria, Belgium, Denmark, Finland, Germany, Greece, Ireland, Italy, Japan, Liechtenstein, Malta, Netherlands, New Zealand, Norway, Portugal, Slovakia, Slovenia, Spain, Sweden, Switzerland, United Kingdom.

Recall number Z-3301-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 7, 2026 · Class II · Ongoing

Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number:…

Percussionaire Corporation · Sandpoint, ID, United States

Why: Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation

Product details, where it was sold and what to do

Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number: P5-UC, used with In-Line Valve Instruction Manual

Quantity: 61,858

Distribution: Worldwide - US Nationwide distribution including in the states of CA, PA, OK, GA, TX, OH, WI, WA, NY, MO, FL, DE, LA, SC, WV, NJ, NE, KS, NC, AL, CO, VA, OR, AZ, IL, CT, ID, NH, UT, TN, MD, VT, MS, NV, DC, ME, IA, AR, HI, ND, IN, MT, NM, MN, MI, SD, MA, AK, RI and the countries of Canada, Belgium, Chile, France, Germany, Israel, Italy, Latvia, Netherlands, Norway, Oman, Philippines, Portugal, Qatar, Russia, Saudi Arabia, Spain, Sweden, Switzerland, Turkey, United Arab Emirates, United Kingdom, Kuwait, Australia, South Africa.

Recall number Z-3319-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

What to do if you own a recalled product

  1. Match it exactly. Recalls usually cover specific lot or batch numbers, "best by" dates, model numbers or sizes. Compare every detail on your product with the notice.
  2. Stop using it. For food and medicine, do not eat, take or give it to pets, even if it looks and smells fine: Listeria and Salmonella do not change how food looks.
  3. Follow the remedy. Most recalls offer a refund, repair or replacement. Return food to the store or follow the company's instructions; for products, contact the company named in the notice.
  4. Do not stop a prescription medicine on your own. Ask your pharmacist or doctor first. They can swap you to an unaffected batch.
  5. Report problems. In the U.S., report illnesses from food or medicine to FDA MedWatch and injuries from products to SaferProducts.gov.

Beware of recall scams

Criminals send fake "recall refund" texts and emails that ask you to pay a "shipping fee" or enter card details. Real recalls never ask for payment. Paste any suspicious recall message into our scam text checker. Read more: Product recalls: how they work and what to do.

Sources: U.S. Food and Drug Administration Enforcement Reports (via openFDA) and the U.S. Consumer Product Safety Commission recall database. FDA enforcement reports list recalls when they are classified, which can be a few weeks after the company's first announcement. Vehicle recalls are available per vehicle in our VIN check.