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. 2,862 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,862 in last 12 months

Showing 34013420 of 53,621 recalls

DrugFebruary 4, 2025· AvKARE

Recalled Item: Silodosin Capsules Recalled by AvKARE Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of Specification (OOS) result for De hydro Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2025· Angiodynamics, Inc.

Recalled Item: IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit...

The Issue: Product is mislabeled with the incorrect fill volume.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2025· Instrumentation Laboratory

Recalled Item: HemosIL LMW Heparin Controls Recalled by Instrumentation Laboratory Due to...

The Issue: Multiple complaints indicating lower than expected quality control (QC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2025· St. Jude Medical

Recalled Item: CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital...

The Issue: Due to issues associated with data migration of patient information and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2025· Beckman Coulter, Inc.

Recalled Item: Access Erythropoietin (EPO) Recalled by Beckman Coulter, Inc. Due to...

The Issue: Affected lot (439363) exhibited a negative dose drop of -22% with native...

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

Class II — Potential Health HazardOngoing
FoodJanuary 31, 2025· Turkana Food Inc.

Recalled Item: Aleppo Tahini Sesame Paste Recalled by Turkana Food Inc. Due to Potential...

The Issue: Product tested positive for Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 31, 2025· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana Recalled by...

The Issue: Firm received complaints of infant choking.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 31, 2025· Nestle-USA, Inc. (Corporate Office)

Recalled Item: Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Recalled...

The Issue: Firm received complaints of infant choking.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 31, 2025· Alvogen, Inc

Recalled Item: Fentanyl Transdermal System CII Recalled by Alvogen, Inc Due to Defective...

The Issue: Defective delivery system - patches could be multi-stacked, adhered one on...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...

The Issue: The forceps have been used in ways not covered by the design resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR355 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...

The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm and MMT-715 Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...

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

Class II — Potential Health HazardOngoing