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Consumer Product Recalls

127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.

April 24, 2025VehiclesNHTSA
Chevrolet, Gmc, Cadillac 2021–2024 Engine And Engine Cooling recall
Hazard: Engine failure increases the risk of a crash.
April 24, 2025ToysCPSC
Huffy Recalls Torex UTV Ride-On Toys Due to Fire Hazard; Sold Exclusively at Walmart
Hazard: The recalled ride-on toys can overheat due to improper wiring, posing a fire hazard.
April 24, 2025Bikes & Recreational VehiclesCPSC
Kawasaki Motors USA Recalls Model Year 2025 Competition and Cross-Country Motorcycles Due to Crash Hazard
Hazard: The primary gear for the crank shaft can fail, posing a crash hazard.
April 24, 2025Children's ProductsCPSC
Deals Oasis Recalls Shape Sorter Car Toys Due to Choking Hazard; Violation of Small Parts Requirements; Risk of Serious Injury or Death
Hazard: The recalled shape sorter car toys contain balls that violate regulations banning small parts in toys intended for children under three years of age because they are a choking hazard, and can cause serious injury or death.
April 24, 2025ToysCPSC
Huffy Recalls Children's Ride-On Tonka Dump Trucks Due to Fire and Burn Hazards Sondiko Butane Torches Recalled Due to Risk of Serious Injury or Death from Burn and Fire Hazards; Violation of Federal Regulations for Multipurpose Lighters; Sold on Amazon by Sondikodirt
Hazard: The recalled butane torches violate the mandatory federal regulations for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk of serious burn injuries or death to children.
April 24, 2025ToysCPSC
Huffy Recalls Children's Ride-On Tonka Dump Trucks Due to Fire and Burn Hazards
Hazard: The controller on the recalled ride-on dump trucks can overheat, posing fire and burn hazards.
April 24, 2025OtherCPSC
Roll Up Window Blinds Recalled Due to Risk of Serious Injury or Death from Strangulation and Entanglement Hazards; Violation of Federal Regulations for Window Coverings; Sold Exclusively on Amazon.com by BTAMREE
Hazard: The recalled window blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window blinds are in violation of the federal regulations for window coverings and present a substantial product hazard.
April 24, 2025OtherCPSC
Window Roll Up Shades Recalled Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violation of Federal Regulations for Window Coverings; Sold Exclusively on SHEIN.com by LuckupShein
Hazard: The recalled window shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window shades are in violation of the federal regulations for window coverings and present a substantial product hazard. The window shades also violate federal regulations for labeling of window coverings.
April 24, 2025Lighting & ElectricalCPSC
AliExpress Recalls LED Strip Lights Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Reese's Law Federal Safety Regulations for Consumer Products with Coin Batteries; Sold on AliExpress.com
Hazard: The recalled lights violate the mandatory federal regulations for consumer products designed to use button cell or coin batteries because the strip lights allow easy access by children to the lithium coin batteries, posing an ingestion hazard. In addition, the recalled products do not have the required warnings. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
April 23, 2025Medical DevicesFDA
Stryker GmbH recalls Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
Hazard: The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
April 23, 2025Medical DevicesFDA
Stryker GmbH recalls Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;
Hazard: The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHR
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Refer to RES
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) BASIC CATARACT, Model Number: DYNJ41097A; 2) PK EYE, Model N
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK, Model Number: DYNJ68673; 2) D AND C PAC
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) PERI GYN PACK, Model Number: DYNJ80786; 2) D & C HYSTEROSCOP
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) ED CRASH C-SECTION TRAY, Model Number: MNS13635A; 2) C-SECTI
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2) NHS - LAP BOWEL GN
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAG
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NEURO PACK WRO-LF, Model Number: DYNJ41856C; 2) STIM IMPLANT
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) UNIVERSAL DRAPE PACK, Model Number: DYNJCD0239
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) CSTM PACEMAKER DRAPE PACK, Model Number: DYNJCD0339
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) IV PACK SOUTH, Model Number: DYNJ88422
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) PRECIP TRAY, Model Number: MNS12590
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Refer to RES
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
April 23, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) MINOR BASIN -SMH, Model Number: DYNJ907733B
Hazard: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.