Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,820 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,820 in last 12 months

Showing 92219240 of 53,621 recalls

Medical DeviceJune 5, 2023· Luminex Corporation

Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Recalled by Luminex...

The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· B. Braun Medical, Inc.

Recalled Item: Perifix¿ / Epidural anesthesia kit (10 count carton) Recalled by B. Braun...

The Issue: Kits were assembled with the incorrect Filter Straw.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2023· Covidien, LLC

Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...

The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2023· Beckman Coulter Biomedical GmbH

Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...

The Issue: A software defect in the DxA Automation System may cause tests to be run on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2023· Beckman Coulter Biomedical GmbH

Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...

The Issue: A software defect in the DxA Automation System may cause tests to be run on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJune 1, 2023· Amin Trading Agency LLC

Recalled Item: Everest Garam Masala Recalled by Amin Trading Agency LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Amin Trading Agency LLC

Recalled Item: Everest Sambhar Masala Recalled by Amin Trading Agency LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Amin Trading Agency LLC

Recalled Item: Maggi Masala ae Magic Recalled by Amin Trading Agency LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Julian's Recipe, LLC

Recalled Item: Julian's Recipe Maple & Brown Butter Cauli-Wafels Recalled by Julian's...

The Issue: Contains undeclared soy lecithin

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Julian's Recipe, LLC

Recalled Item: Julian's Recipe Original Cauli-Wafels Recalled by Julian's Recipe, LLC Due...

The Issue: Contains undeclared soy lecithin

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Julian's Recipe, LLC

Recalled Item: Julian's Recipe CAULI-WAFEL SANDWICHES TURKEY SAUSAGE & CHEDDAR Recalled by...

The Issue: Contains undeclared soy lecithin

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugMay 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg Recalled by The Harvard Drug Group...

The Issue: Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund