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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.

Latest recalls

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

Passport Series Patient Monitor

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

Passport Series Patient Monitor. Operator's Manuals: 8 / 12 / 12M / 17M / V

Quantity: 39,891 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0114-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

HEART PREP 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

HEART PREP TRAY; Model/Item Number (Kit): MECV97W;

Quantity: 96

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

Recall number Z-0102-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

PACK OPEN HEART CFH

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

PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;

Quantity: 124

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

Recall number Z-0097-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

TufTex¿ Over-the-Wire Embolectomy Catheter

LeMaitre Vascular, Inc. · Burlington, MA, United States

Why: Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.

Product details, where it was sold and what to do

TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;

Quantity: 54

Distribution: US Nationwide distribution in the states of CA, FL, GA, KY, LA, NJ, OH, PA, SC.

Recall number Z-0117-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

T1 Patient Monitor

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

T1 Patient Monitor. Operator's Manual: T1 Patient Monitor

Quantity: 4,946 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0116-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Sperm Ab ELISA

DRG International, Inc. · Springfield, NJ, United States

Why: Potential for false negative patient results.

Product details, where it was sold and what to do

Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);

Quantity: 211

Distribution: Worldwide - US Nationwide distribution in the state of NJ and the countries of Azerbaijan, Belgium, Czech Republic, Germany, Hungary, India, Italy, Kuwait, Russia, Spain, Ukraine.

Recall number Z-0082-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Po…

Intellijoint Surgical, Inc. · Kitchener, N/A, Canada

Why: A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat and pose a fire safety risk.

Product details, where it was sold and what to do

Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP, Portable System, REF: 000-0249

Quantity: 8

Distribution: Worldwide - US Nationwide distribution in the states of CA, TX, MS, NJ and the countries of Singapore, Spain.

Recall number Z-0119-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number: 804-33-300 (Enovis)

QUANTUM OPS Inc · Chattanooga, TN, United States

Why: Due to a manufacturing issue (inadequate weld) for patient head positioning system.

Product details, where it was sold and what to do

Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number: 804-33-300 (Enovis); 3105-400-030 (Stryker); internal BC-0001 / BC-0220 Software Version: N/A Product Description: Surgical beach-chair positioner that mounts to the accessory rails of the OR table leg section to elevate and support the patient's upper body in the upright (beach chair) position during surgical procedures. Component: No, finished device. The failure is in the BC-0105, subcomponent.

Quantity: 266

Distribution: U.S. Nationwide distribution in the states of CA and TX.

Recall number Z-0076-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

LAPAROSCOPIC PROSTATECTOMY

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

LAPAROSCOPIC PROSTATECTOMY; Model/Item Number (Kit): NIHB0036-07;

Quantity: 15

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

Recall number Z-0099-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

BeneView Series

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

BeneView Series. Operator's Manuals: T5 / T8

Quantity: 133 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0113-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

CPM Series Patient Monitor

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12

Quantity: 1,699 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0115-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No

Beckman Coulter Inc. · Brea, CA, United States

Why: Beckman Coulter has identified a software issue affecting DxC 500 AU Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use units different from the system default, a subsequent configuration change and activation of the draft configuration in the System Configuration page may cause the analyzer to revert the test units to the system default setting without n…

Product details, where it was sold and what to do

DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No. C63519 2. AU w/ISE, Part No. C63520

Quantity: 146 US, 170 OUS

Distribution: Worldwide - US Nationwide distribution.

Recall number Z-0084-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Alphenix INFX-8000C/B5

Canon Medical System, USA, INC. · Tustin, CA, United States

Why: Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motion error

Product details, where it was sold and what to do

Alphenix INFX-8000C/B5

Quantity: 1 unit

Distribution: US Nationwide distribution in the state of ID.

Recall number Z-0108-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

HALYARD Laparoscopy Comprehensive Pack II REF: 49332

GRI Medical & Electronic Technology Co., Ltd. · Jia Xing, N/A, China

Why: Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter

Product details, where it was sold and what to do

HALYARD Laparoscopy Comprehensive Pack II REF: 49332

Quantity: 396 kits

Distribution: US Nationwide distribution in the state of MS.

Recall number Z-0077-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

ENDOVASCULAR PACK

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

ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;

Quantity: 33

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

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

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

BeneVision Series Telemetry Monitor

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80

Quantity: 29,737 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0111-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

DAVINCI LAP/GYN

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

DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;

Quantity: 30

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

Recall number Z-0101-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

SEDIPLAST

POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC · Cortlandt Manor, NY, United States

Why: During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be forcibly ejected, potentially resulting in the release of blood and exposure of the operator or surrounding work area to a biological hazard (blood).

Product details, where it was sold and what to do

SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;

Quantity: 448400

Distribution: Worldwide - US Nationwide distribution in the states and territory of AK, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WV and the country of United Kingdom.

Recall number Z-0107-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No

Beckman Coulter Inc. · Brea, CA, United States

Why: Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a Clinical Chemistry test to use units different from the system default, a subsequent configuration change and activation of the draft configuration in the System Configuration page may cause the analyzer to revert the test units to the system default setting without not…

Product details, where it was sold and what to do

DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No. C63522 2. DxC 500 AU Module, DxC 500i, Part No. C63521 3. Access 2 Module, DxC 500i, Part No. C13252

Quantity: 146 US, 170 OUS

Distribution: Worldwide - US Nationwide distribution.

Recall number Z-0083-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085 AN2336608H AN2336608J Int…

Cardinal Health 200, LLC · Waukegan, IL, United States

Why: Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the patient's endotracheal tube to perform a procedure. The issue can result in a delay to treatment and unintended extubation. The potential exists for respiratory failure, hypoxia, aspiration, or low oxygen saturation.

Product details, where it was sold and what to do

Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366085 AN2336608H AN2336608J Intubating Bag Kit Catalog Number OMSVM4166A Intubation UH Kit Catalog Number AN2336608G

Quantity: 210 total kits

Distribution: Pending

Recall number Z-0079-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Panorama and Telemetry Monitoring System

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).

Quantity: 11,831 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0112-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

MAJOR PACK

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

MAJOR PACK; Model/Item Number (Kit): NIHB0018-11;

Quantity: 40

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

Recall number Z-0104-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 208…

Medical Action Industries, Inc. 306 · Arden, NC, United States

Why: An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.

Product details, where it was sold and what to do

Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 20809160118228 Software Version: N/A

Quantity: 4000

Distribution: U.S.: CA O.U.S.: N/A

Recall number Z-0069-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

GYN LAPAROSCOPY/LAPAROTOMY

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

GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;

Quantity: 134

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

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

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

BeneVision N1 and N-Series Patient Monitor

Mindray DS USA, Inc. · Mahwah, NJ, United States

Why: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Product details, where it was sold and what to do

BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12/N15/N17/N19/N22.

Quantity: 44,651 units

Distribution: Worldwide - Nationwide and the country of Canada.

Recall number Z-0110-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

ABD HYSTERECTOMY

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

ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07;

Quantity: 23

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

Recall number Z-0106-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

GYN LAPAROSCOPY PACK

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

GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12;

Quantity: 28

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

Recall number Z-0105-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical purposes to provide mod…

Medline Industries, LP · Northfield, IL, United States

Why: The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the front wheels may become loose or detach from the rollator. If the front wheels become loose or detach during use, there is risk of severe adverse events. The immediate consequences could include falls resulting in head trauma, bone fracture…

Product details, where it was sold and what to do

Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWS

Quantity: 1824 units

Distribution: Worldwide distribution - US Nationwide and the country of Canada.

Recall number Z-0086-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

VERIFY Biological Steam Test Pack Model/Catalog Number: S3069

Steris Corporation · Mentor, OH, United States

Why: Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction

Product details, where it was sold and what to do

VERIFY Biological Steam Test Pack Model/Catalog Number: S3069

Quantity: 233

Distribution: Worldwide - US Nationwide distribution.

Recall number Z-0075-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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

DAVINCI TRUCUSTOM BUNDLE

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

DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;

Quantity: 144

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

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

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What to do if you own a recalled product

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.
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.
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.
Do not stop a prescription medicine on your own. Ask your pharmacist or doctor first. They can swap you to an unaffected batch.
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.