United States Recalls

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

Showing 24 of 16,532 results
TOMY Recalls Boon NURSH 8 oz Reusable Baby Bottles Due to Choking Hazard; Sold a...
CPSCGeneral Alert

TOMY Recalls Boon NURSH 8 oz Reusable Baby Bottles Due to Choking Hazard; Sold a...

The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children.

Jun 4, 2026
Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death...
CPSCGeneral Alert

Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death...

The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows?and infant support cushions?because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.

Jun 4, 2026
Tiny Land Children's Play Tents Recalled Due to Risk of Injury from Irritation t...
CPSCGeneral Alert

Tiny Land Children's Play Tents Recalled Due to Risk of Injury from Irritation t...

The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation.

Jun 4, 2026
Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury f...
CPSCGeneral Alert

Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury f...

The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium?ion battery's metal casing, causing the battery to rapidly overheat, posing a risk of serious injury or property damage from fire and burn hazards.

Jun 4, 2026
Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard
CPSCGeneral Alert

Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard

The recalled heater's fan blade can detach from the motor shaft, which can cause the fan to slow or stop, leading to overheating and melting of the enclosure and internal parts. Melted internal parts can ignite and breach the enclosure if the thermal cut off or fuse does not timely activate, posing a fire hazard.

Jun 4, 2026
Food & Beverage
FDA FoodClass I

Wawa Fruit Punch Pint (16oz), Plastic bottle

Undeclared Milk Allergen,

Jun 3, 2026Wawa Beverage Company
Food & Beverage
FDA FoodClass I

giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt ...

Products were made with recalled California Dairies milk powder due to Salmonella.

Jun 3, 2026Legacy Bakehouse LLC
Medical Device
FDA DevicesClass II

Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ2162...

Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister pack are labeled as a 1 mL Luer Lock Tuberculin Syringe (Product Code 1180100777), but the syringes inside are U-100 insulin syringes.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS),...

Nitrile Exam Glove failed to meet specifications chemical permeation performance.

Jun 3, 2026O&M HALYARD INC
Medical Device
FDA DevicesClass II

GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; u...

GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

Jun 3, 2026GE Medical Systems Information Technologies Inc
Medical Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product...

GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

Jun 3, 2026GE Medical Systems Information Technologies Inc
Medical Device
FDA DevicesClass II

Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimul...

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

Jun 3, 2026Medtronic Neuromodulation
Medical Device
FDA DevicesClass II

Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimul...

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

Jun 3, 2026Medtronic Neuromodulation
Food & Beverage
FDA FoodClass I

(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099

Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.

Jun 3, 2026Honeyville, Inc
Vehicle
NHTSAELECTRICAL SYSTEM

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 10...

The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.

Jun 3, 2026Jayco, Inc.
Medical Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orde...

GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

Jun 3, 2026GE Medical Systems Information Technologies Inc
Pharmaceutical
FDA DrugsClass III

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Steril...

Failed Stability Specifications

Jun 3, 2026AbbVie Inc.
Vehicle
NHTSAELECTRICAL SYSTEM

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 10...

The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.

Jun 3, 2026Jayco, Inc.
Vehicle
NHTSASERVICE BRAKES,...

Aston Martin The Americas - Brake Master Cylinder Seal May Deform

Brakes that overheat increase the risk of a fire.

Jun 3, 2026Aston Martin The Americas
Medical Device
FDA DevicesClass II

HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3

Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.

Jun 3, 2026Devicor Medical Products Inc
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