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. 2,653 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,653 in last 12 months

Showing 2632126340 of 53,621 recalls

DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 17, 2018· Neighbors LLC

Recalled Item: Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2...

The Issue: Undeclared almonds on the labeling

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 17, 2018· Blommer Chocolate Co., Inc.

Recalled Item: Blommer Natural Cocoa Butter Bulk Tanker Recalled by Blommer Chocolate Co.,...

The Issue: CCP process deviation, Critical limit not met

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 15, 2018· TriMed Inc.

Recalled Item: TriMed Olecranon Hook Plate Recalled by TriMed Inc. Due to The firm has...

The Issue: The firm has become aware that the angled-hole of certain semi-tubular...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System- (). For use in the in Recalled by...

The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System-For use in the in vitro quantitative Recalled...

The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...

The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...

The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Permobil, Ab

Recalled Item: Permobil powered wheelchairs Recalled by Permobil, Ab Due to This correction...

The Issue: This correction decision has been made because of a potential failure of one...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Agilent Technologies, Inc.

Recalled Item: MassHunter Quantitative Analysis Software Recalled by Agilent Technologies,...

The Issue: When utilizing specific software versions of an LC/MS device, and Batch at a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Agfa N.V.

Recalled Item: DX-D 600 Product Usage: The DX-D 600 system is a Recalled by Agfa N.V. Due...

The Issue: A supplier for the Agfa system noted a potential for the steel support...

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

Class II — Potential Health HazardOngoing
DrugAugust 15, 2018· Hetero Labs Limited Unit V

Recalled Item: Montelukast Sodium Tablets 10 mg Recalled by Hetero Labs Limited Unit V Due...

The Issue: Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2018· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

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

Class III — Low RiskOngoing
Refund