Updated 8 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

Medical devices · Oct 21, 2026 · Class II · Ongoing

Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D

Medline Industries, LP · Northfield, IL, United States

Why: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Product details, where it was sold and what to do

Medline surgical convenience kits labeled as: VEIN HARVESTING PACK, Medline product number/SKU DYNJ51845D

Quantity: 56 kits

Distribution: US Nationwide distribution.

Recall number Z-0172-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D

Medline Industries, LP · Northfield, IL, United States

Why: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Product details, where it was sold and what to do

Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D

Quantity: 165 kits

Distribution: US Nationwide distribution.

Recall number Z-0178-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M

Medline Industries, LP · Northfield, IL, United States

Why: Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

Product details, where it was sold and what to do

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M

Quantity: 3,551 kits

Distribution: US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.

Recall number Z-0184-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Medline convenience kit labeled as: FOOT ANKLE

Medline Industries, LP · Northfield, IL, United States

Why: Discrepancy in the shelf-life of a component

Product details, where it was sold and what to do

Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A

Quantity: 30 kits

Distribution: US Nationwide distribution in the state of NY.

Recall number Z-0189-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone ma…

Medtronic Sofamor Danek USA Inc · Memphis, TN, United States

Why: Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the presence of microbial organisms. While the batch passed finished product sterility testing Medtronic is retrieving any unused product manufactured from the donor tissue. Donor bone tissue tested positive for Clostridium butyricum and while tissue did und…

Product details, where it was sold and what to do

Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with an inert additive to yield a demineralized bone matrix (DBM) allograft product having a particular physical form and/or handling property. Grafton DBM Gel and Grafton Plus DBM Paste are produced from a powder form of DBM, while Grafton DBM Flex, Putty, Matrix, Crunch" and Orthoblend are produced from a fiber form of DBM Crunch" also contains demineralized bone chips/cubes, while Grafton DBM Orthoblend contains non-demineralized cancellous bone chips in addition to DBM. Grafton DBM and Grafton Plus DBM are malleable and can be molded or cut into various sizes and shapes according to the intended implant site.

Quantity: 20

Distribution: US Nationwide distribution in the states of OK, VA, CO, AR, FL, TX, MD, DE, IL, MI, KS, AL, GA.

Recall number Z-0138-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder wall, Reference Part Num…

Cook Incorporated · Bloomington, IN, United States

Why: The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing. Potential events that may occur as a result of this issue include increased procedural time and inadequate treatment.

Product details, where it was sold and what to do

Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder wall, Reference Part Number 090001-S26, Order Number (GPN) G16112

Quantity: 97 units

Distribution: US States: FL, IL, NM, TX, WA. Canada, France, Germany, Italy, Spain, Switzerland.

Recall number Z-0163-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class I · Ongoing

HemoslL AcuStar HIT-lgG(PF-4)

Instrumentation Laboratory · Bedford, MA, United States

Why: Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples.

Product details, where it was sold and what to do

HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only)

Quantity: 1,414 units

Distribution: Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, FL, GA, MA, MD, NJ, NY, PA, RI, TN, WA, WV and the countries of Austria, Belgium, Switzerland, Costa Rica, Czech Republic, Germany, Denmark, Spain, Finland, France, United Kingdom, Greece, India, Italy, Jordan, Japan, South Korea, Luxembourg, Latvia, Netherlands, Saudi Arabia, Sweden, Singapore.

Recall number Z-0002-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L

Medline Industries, LP · Northfield, IL, United States

Why: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Product details, where it was sold and what to do

Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2) OPEN HEART ACCESSORY PACK, Medline Product number/SKU DYNJT5715A; 3) CABG ACCESSORY PACK, Medline Product number/SKU DYNJ85751; 4) OPEN HEART PACK, Medline Product number/SKU DYNJ53741N; 5) OPEN HEART PACK 1&2, Medline Product number/SKU DYNJ80701A; 6) VEIN PACK, Medline Product number/SKU DYNJ67308C; 7) OPEN HEART PACK, Medline Product number/SKU DYNJ89451B; 8) VASCULAR TRAY-LF, Medline Product number/SKU DYNJ42166A; 9) ENDOSCOPIC VEIN HARVEST PK, Medline Product number/SKU DYNJ67363C; 10) ENDOSCOPIC VEIN HARVEST PK, Medline Product number/SKU DYNJ67363B; 11) LIVER TRANSPLANT PACK B, Medline Product number/SKU DYNJ65779B; 12) CABG PACK-LF, Medline Product number/SKU DYNJ47661J; 13) VEIN HARVEST PACK, Medline Product number/SKU DYNJ04470L; 14) CARDIAC PACK, Medline Product number/SKU DYNJ44647D; 15) GM OPEN HEART ACC PACK-LF, Medline Product number/SKU DYNJ0660029AM; 16) CARDIOVASCULAR PACK-LF, Medline Product number/SKU DYNJ0160327C; 17) GOOD SHEPHERD OPEN HEART, Medline Product number/SKU DYNJ60819L; 18) OPEN HEART PACK, Medline Product number/SKU DYNJ0271227R; 19) OPEN HEART PACK, Medline Product number/SKU DYNJ81541C; 20) TAVR PACK, Medline Product number/SKU DYNJ54094F; 21) TRANSPLANT BACKTABLE PACK, Medline Product number/SKU DYNJ62055C; 22) VASCULAR, Medline Product number/SKU DYNJ49366; 23) BACK TABLE TRAY, Medline Product number/SKU DYNJ65416D; 2…

Quantity: 36199 kits

Distribution: US Nationwide distribution.

Recall number Z-0176-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Triathlon Hinge Femoral Prep Tray

Howmedica Osteonics Corp. · Mahwah, NJ, United States

Why: Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.

Product details, where it was sold and what to do

Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514.

Quantity: 359 trays

Distribution: These trays are provided by sale or loan. Loans are provided through Distributor. Foreign Consignees will be identified by the countries impacted. 158 trays have been distributed OUS.

Recall number Z-0166-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Power F2 Powered Fastening System, Power F2, Item No

Ferno-Washington Inc · Wilmington, OH, United States

Why: Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system not operating in powered mode, or exhibiting reduced powered performance. Issue may result in interruption or delay in patient transport.

Product details, where it was sold and what to do

Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816 and PowerX2 Premium, Item No. 0015821

Quantity: 319

Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, ID, IL, KY, LA, ME, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI, WV and the countries of Netherlands and Poland.

Recall number Z-0145-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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Medical devices · Oct 21, 2026 · Class II · Ongoing

TS Universal Baseplate Finishing Tray, Triathlon

Howmedica Osteonics Corp. · Mahwah, NJ, United States

Why: Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.

Product details, where it was sold and what to do

TS Universal Baseplate Finishing Tray, Triathlon. Catalog Number: 6543-6-506.

Quantity: 605 trays

Distribution: These trays are provided by sale or loan. Loans are provided through Distributor. Foreign Consignees will be identified by the countries impacted. 158 trays have been distributed OUS.

Recall number Z-0164-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Oct 21, 2026 · Class II · Ongoing

Tirzepatide/Niacinamide 2mL vial (40 MG per Vial) Inj 20mg/2mg/mL

Houston Rx LLC · Houston, TX, United States

Why: Lack of assurance of sterility.

Product details, where it was sold and what to do

Tirzepatide/Niacinamide 2mL vial (40 MG per Vial) Inj 20mg/2mg/mL, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032.

Quantity: 64 vials

Distribution: Nationwide in the USA.

Recall number D-0040-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Oct 21, 2026 · Class II · Ongoing

Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial

Zydus Pharmaceuticals (USA) Inc · Pennington, NJ, United States

Why: Failed Impurities/Degradation Specifications.

Product details, where it was sold and what to do

Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara - 391510 India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1907-1.

Quantity: 70776 vials

Distribution: Nationwide within the United States

Recall number D-0039-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Oct 21, 2026 · Class II · Ongoing

Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10)

American Health Packaging · Columbus, OH, United States

Why: Presence of Foreign Tablets/Capsules

Product details, where it was sold and what to do

Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-620-01; NDC Unit Dose: 60687-620-11

Quantity: 5,363 cartons

Distribution: US Nationwide

Recall number D-0042-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Oct 21, 2026 · Class II · Ongoing

Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle

Teva Pharmaceuticals USA, Inc · Parsippany, NJ, United States

Why: Presence of Foreign Tablets/Capsules

Product details, where it was sold and what to do

Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC 100 Tablets: 0093-2204-01; NDC 500 Tablets: 0093-2204-05

Quantity: 240,448 cartons

Distribution: US Nationwide.

Recall number D-0038-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Oct 21, 2026 · Class II · Ongoing

Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution

Houston Rx LLC · Houston, TX, United States

Why: Lack of process control

Product details, where it was sold and what to do

Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032.

Quantity: 7 vials

Distribution: Nationwide in the USA.

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

Food · Oct 21, 2026 · Class I · Ongoing

Deano's Pasta

DEANO'S PASTA · Somerville, MA, United States

Why: Undeclared Lobster

Product details, where it was sold and what to do

Deano's Pasta; Pear and Pecorino Triangoli Ravioli, 1lb.; Ingredients: Dough: Semolina (Wheat, Niacin, Thiamine, Mononitrate, Riboflavin, Folic Acid), Water, Fresh Eggs, Salt. Filling: Pears, Ricotta (Whey, Cream, Milk), Pecorino Cheese (Milk, Cultures, Salt, Enzymes), Breadcrumbs (Wheat Flour, Cane Sugar, Yeast, Salt), Brandy, Dark Brown Sugar, Salt, Black Pepper.; CONTAINS: WHEAT, MILK, EGG ingredients; MAY CONTAIN OTHER ALLERGENS; KEEP FROZEN

Quantity: 78lbs

Distribution: MA, NH

Recall number H-0092-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 21, 2026 · Class II · Ongoing

Holsum Spinach Flour Tortillas Large, 8 count (20 oz.)

Holsum De Puerto Rico, Inc. · Toa Baja, PR, United States

Why: Undeclared colors (FD&C Blue No. 1 and FD&C Yellow No. 5)

Product details, where it was sold and what to do

Holsum Spinach Flour Tortillas Large, 8 count (20 oz.) UPC: 810023430629

Quantity: 600.125 boxes (9,602 units)

Distribution: PR, US Virgin Islands

Recall number H-0089-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 21, 2026 · Class II · Ongoing

Stewarts Shops Vanilla chocolate Strawberry Ice Cream 1/2 gallon (1.89 L)

Stewart's Shops Corp. · Saratoga Springs, NY, United States

Why: Foreign object: May contain pieces of metal

Product details, where it was sold and what to do

Stewarts Shops Vanilla chocolate Strawberry Ice Cream 1/2 gallon (1.89 L), UPC: 0 82086 44377 3

Quantity: 10,760 units

Distribution: NY, VT, NH

Recall number H-0093-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 21, 2026 · Class II · Ongoing

Made From Plants

DARING FOODS INC · Long Beach, CA, United States

Why: defective packaging; packaging can rupture/explode during cooking.

Product details, where it was sold and what to do

Made From Plants; Daring; Plant Steak Bites; Ready in 4 Mins Microwaveable Pouch; UPC: 86001124319

Quantity: 4544 cases / 27,324 individual retail units

Distribution: Product was distributed to a single retail grocery chain customer with multiple locations in Florida and one location in North Carolina. A total of 6 locations received recalled product.

Recall number H-0091-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 21, 2026 · Class III · Ongoing

Pur Aqua Sparkling Frost Cherry Limeade 17 oz.

Refresco Beverages US Inc · Tampa, FL, United States

Why: May contain undeclared aspartame.

Product details, where it was sold and what to do

Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 4099100167023

Quantity: 2100 units

Distribution: Florida with further downstream distribution to retail stores

Recall number H-0095-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 21, 2026 · Class II · Ongoing

J

Saratoga Potato Chips LLC · Fort Wayne, IN, United States

Why: Undeclared soy.

Product details, where it was sold and what to do

J. HIGGS Loaded Bacon & Cheddar Potato Chips, NET WT 7.75 OZ (219.7g) bag, UPC 051933316454. Sold as 13 (7.75oz) bags per case.

Quantity: 769 cases (13 bags/case)

Distribution: The recalled J. HIGGS Loaded Bacon and Cheddar Potato Chips were distributed in the states of Florida, Indiana, Kentucky, Ohio, Tennessee, and Maryland and sold in Save A Lot stores.

Recall number H-0090-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 21, 2026 · Class II · Ongoing

Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon (1.89 L)

Stewart's Shops Corp. · Saratoga Springs, NY, United States

Why: Foreign object: May contain pieces of metal

Product details, where it was sold and what to do

Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon (1.89 L), UPC Codes: 0 82086 44371 1

Quantity: 10,392 units

Distribution: NY, VT, NH

Recall number H-0094-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Consumer products · Oct 15, 2026

usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails

Opal Vista Ltd., dba usOpal, of China · China

Why: The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. In addition, …

Product details, where it was sold and what to do

Xalirium Adult Portable Bed Rails. This recall involves Xalirium-branded adult portable bed rails. They have a white frame with black foam rubber grips and a black fabric pouch. The bed rails measure about 17.15 inches high, 4.33 inches wide and 1.99 inches long. "Xalirium" is printed on the label of the product packaging. Only bed rails without vertical bars inside the opening are included in this recall.

Quantity: About 200

Distribution: Sold at Sold Online At: Amazon.com from February 2026 through August 2026 for about $60.

Remedy: Consumers should stop using the recalled adult portable bed rails immediately and contact usOpal for a full refund. Consumers will be asked to cut the black storage bag and straps and to cut the foam padding on the bed rails, write "RECALLED" on the upper and lower bed rails, and send a photo of the marked rails to xaliriumofficial@outlook.com. Consumers should then dispose of the recalled product

Official CPSC recall notice ↗

Consumer products · Oct 15, 2026

Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion

Primark US Corp., of Boston, Massachusetts · China

Why: The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through ingestion, and certain phthalates have been associated with adverse health effects, particularly effects on development and the hormone system.

Product details, where it was sold and what to do

101 Dalmatians Faux Leather Coin Purses. This recall involves the Primark 101 Dalmatians Faux Leather Coin Purse, Model No. 2595301. The coin purse is black and has a picture of a dalmatian and "101 Dalmatians" printed on the front. The model number is located on the product tag attached to the zip puller.

Quantity: About 2,100

Distribution: Sold at Sold At: Primark stores located in the Northeast and in Florida, Maryland and Illinois from March 2026 through June 2026 for about $9.

Remedy: Consumers should stop using the coin purses immediately, keep them away from children and return them to a Primark store for a full refund in the original form of payment.

Official CPSC recall notice ↗

Consumer products · Oct 15, 2026

Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards

Papablic, Inc., doing business as Papablic, of USA, of Chicago, Illinois · China

Why: The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced, causing a baby to become entrapped between the sleeping pad and bottom posing a deadly suffocation hazard. In addition, the latching and locking mechanism can fail, causing the product to collapse, posing a risk of serious injury or deadly entrapment and fall hazards.

Product details, where it was sold and what to do

Papablic Bedside Sleepers with Play Yard Extensions. This recall involves Papablic bedside sleepers, model PAPA03001AI. These convertible sleepers function as both a bassinet and a play yard and have a gray exterior with an interior printed in a stars‑and‑moon pattern. The products have "Papablic" stitched in white on the front gray fabric panel. Model "PAPA03001AI" is printed on a label sewn to the interior fabric of the bassinet underneath the mattress pad.

Quantity: About 248

Distribution: Sold at Sold Online At: Amazon.com and papablic.com from April 2025 through July 2026 for about $190.

Remedy: Consumers should stop using the convertible bedside sleeper immediately and contact Papablic for a refund. Consumers will be asked to disassemble the product, cut the mattress and fabric components in half and email photos of the destroyed components to support@papablic.com. Upon receipt of proof of destruction, Papablic will issue a full refund and consumers should dispose of the product.

Official CPSC recall notice ↗

Consumer products · Oct 15, 2026

Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards

Loving Thyself Rocks LLC, of Winter Park, Florida · China

Why: Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards.

Product details, where it was sold and what to do

Crystal Glass Cups with Loose Crystal Chips. This recall affects Crystal Glass Cups containing loose crystal stone chips between two layers of glass. The cups are intended for both decorative use and drinking. Each cup measures approximately 3.5 by 3 inches. The crystal stone chips are sold in various options: amethyst, black obsidian, rose quartz, smoke quartz, fire and clear quartz, moss agate, hematite, black tourmaline, black tourmaline in quartz, charoite, blue apatite, morganite, larimar, red jasper, malachite, garnet, kunzite, fluorite, peridot, aquamarine, watermelon tourmaline, carnelian, lapis lazuli, tigers eye and labradorite.

Quantity: About 600

Distribution: Sold at Sold At: Loving Thyself store and on-line at https://www.instagram.com/lovingthyselfrocksandfossils/?hl=en and https://www.instagram.com/lovingthyselfrocks/?hl=en and Etsy.com from April 2026 through September 2026 for between $20 and $50.

Remedy: Consumers should stop using the recalled crystal cup immediately and register at http://www.lovingthyselfrocks.com/recall to receive a full refund in the form of original payment. Consumer will be asked to fill out an online form and submit a photograph with the word "RECALL" written on the front of the crystal cup in permanent black marker. Consumers will be asked to attest to proper disposal of

Official CPSC recall notice ↗

Consumer products · Oct 15, 2026

HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard

HatsanUSA, Inc., of Bentonville, Arkansas · Turkey

Why: The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from projectile hazard.

Product details, where it was sold and what to do

Blitz and Blitz 777 air rifles. This recall involves all units of the Hatsan Blitz and Blitz 777 pellet shooting air rifles sold from February 2020 through March 2026. Both the Blitz and Blitz 777 pellet air rifles were sold in .22, .25 and .30 calibers. The pellet air rifles are gas operated and select-fire (semi-auto/full-auto) pre-charged pneumatic (PCP). They are black and feature a synthetic stock, a carbon fiber air tank mounted beneath the barrel and a rotary magazine feed. Serial numbers and manufacturing dates are engraved on the right side of the receiver above the bolt. On the left side of the receiver is the Hatsan logo, featuring a circular mark, with the word "HATSAN" next to a graphic of a bow and arrow. The model name "BLITZ" or "BLITZ 777" is also marked on the left side of the receiver.

Quantity: About 16,170

Distribution: Sold at Sold At: In store and online at various sporting goods stores and gun shops nationwide, online at hatsanairgunsusa.com and catalog sales including Utah Airguns, Airgun Depot and Pyramyd Air from February 2020 through March 2026 for between $800 and $1,100.

Remedy: Consumers should stop using the recalled air rifles immediately, make sure they are unloaded and contact HatsanUSA for a free trigger assembly replacement which will be mailed along with instructions. If the consumer does not want to complete the replacement of the air rifle trigger assembly on their own, HatsanUSA will provide a prepaid package to ship the product to HatsanUSA for inspection and

Official CPSC recall notice ↗

Consumer products · Oct 15, 2026

3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard

3M Company, of St. Paul, Minnesota · China

Why: The recalled thermal laminators can overheat, posing a fire hazard.

Product details, where it was sold and what to do

Scotch™ Thermal Laminators. This recall involves the Scotch™ thermal laminator, model number TL1302Z. The laminator is light gray/white with gray accents and the word "Scotch" is printed in gray on the front. The laminating slot is approximately 13 inches wide, and the machine has a carrying handle on the right side of the machine when viewing from the front. The model number TL1302Z is located on the sticker on the bottom of the laminator and can also be found on the product packaging.

Quantity: About 53,634

Distribution: Sold at Sold Online At: Amazon.com from June 2024 through September 2026 for between $44 and $56.

Remedy: Consumers should stop using and unplug the recalled thermal laminators immediately and contact 3M Company to receive a full refund. Consumers will be asked to fill out the online recall registration form at https://www.scotchbrand.com/3M/en_US/scotch-brand/tl1302Z-laminator-recall/, confirm that their laminator is included in the recall and upload a photograph of the laminator with the unplugged p

Official CPSC recall notice ↗

Medical devices · Oct 14, 2026 · Class II · Ongoing

PLASTICS TRAY

AVID Medical, Inc. · Toano, VA, United States

Why: Product may be potentially contaminated with a lubricant used during the manufacturing process.

Product details, where it was sold and what to do

PLASTICS TRAY; Model/Item Number (Kit): EURO053;

Quantity: 28

Distribution: US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.

Recall number Z-0100-2027 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.