United States Recalls

Consumer recalls from the FDA, CPSC, NHTSA, and USDA FSIS.

Showing 24 of 16,533 results
Superbobi Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from...
CPSCGeneral Alert

Superbobi Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from...

The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.

May 14, 2026Shenzhen Jiangtou Technology Co., Ltd., dba Remy&shop
BRP Recalls Can-Am All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury and...
CPSCGeneral Alert

BRP Recalls Can-Am All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury and...

The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard.

May 14, 2026
Cosyland Children's Tower Stools Recalled Due to Risk of Serious Injury and Deat...
CPSCGeneral Alert

Cosyland Children's Tower Stools Recalled Due to Risk of Serious Injury and Deat...

The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.

May 14, 2026
World Bright International Limited Recalls Agio Menlo Woven Patio Swings Due to ...
CPSCGeneral Alert

World Bright International Limited Recalls Agio Menlo Woven Patio Swings Due to ...

The swing seat can detach from the frame while in use, posing a risk of serious injury or death from a fall hazard.

May 14, 2026
ZWILLING J. A. Henckels Aktiengesellschaft Recalls Electric Water Kettles Due to...
CPSCGeneral Alert

ZWILLING J. A. Henckels Aktiengesellschaft Recalls Electric Water Kettles Due to...

The kettle's handle can loosen and separate from the kettle, causing hot contents to spill, posing a risk of serious injury due to a burn hazard.

May 14, 2026ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany
Minka Lighting Group Recalls Bardon Series Pendant Light Fixtures Due to Risk of...
CPSCGeneral Alert

Minka Lighting Group Recalls Bardon Series Pendant Light Fixtures Due to Risk of...

The recalled light fixture's frame can detach from the pendant downrod during installation, posing a risk of serious injury or death from an impact hazard.

May 14, 2026
Tiyol Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death ...
CPSCGeneral Alert

Tiyol Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death ...

The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress and becoming a deadly choking hazard.

May 14, 2026
Petzl America Recalls SIMBA and SWAN EASYFIT Harnesses Due to Risk of Serious In...
CPSCGeneral Alert

Petzl America Recalls SIMBA and SWAN EASYFIT Harnesses Due to Risk of Serious In...

The recalled harnesses are missing rivets in the FAST LT PIN-LOCK buckles, causing the buckles to open, posing a risk of serious injury or death from a fall hazard.

May 14, 2026
Food & Beverage
FDA FoodClass I

RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOL...

Multi-state outbreak of E. coli O157:H7.

May 13, 2026Raw Farm LLC
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) SCC RF PAIN MGMT, Model Number:DYNJ56436A; 2) SC...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline Surgical Drapes: 1) SHEET,DRAPE,40X58,STERILE, Model Number: DYNJP2410;...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Pharmaceutical
FDA DrugsClass II

Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. b...

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

May 13, 2026Breckenridge Pharmaceutical, Inc.
Medical Device
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog ...

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

May 13, 2026Katalyst Surgical, LLC
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) OB KIT, Model Number: DYKM2326; 2) KIT LABOR DEL...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc ...

Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.

May 13, 2026Centinel Spine, Inc.
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS, Model Number: CDS98...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Modu...

Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).

May 13, 2026Spacelabs Healthcare, Inc.
Food & Beverage
FDA FoodClass II

Loard's Chocolate Marble Ice Cream - 32 oz

Undeclared Milk.

May 13, 2026Silver Moon LP dba Loard's Ice Cream
Food & Beverage
FDA FoodClass II

Loard's Lemon Chiffon Ice Cream - 32 oz

Undeclared Milk, Eggs, Yellow #5.

May 13, 2026Silver Moon LP dba Loard's Ice Cream
Medical Device
FDA DevicesClass I

Halyard CATH LAB kit. Model Number: SACL75AM.

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

May 13, 2026AVID Medical, Inc.
Medical Device
FDA DevicesClass II

One Step 10A in vitro diagnostic test

The devices were distributed without required FDA premarket clearance or approval.

May 13, 2026DFI Co., Ltd.
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185; 2) LITH...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Pharmaceutical
FDA DrugsClass II

Duloxetine Delayed-Release Capsules, 60 mg, Rx Only, 30 capsules, Marketed by: A...

CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.

May 13, 2026Ajanta Pharma Ltd.
Food & Beverage
FDA FoodClass II

Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 1...

Undeclared allergens (sesame and soy)

May 13, 2026Target Corporation
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