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. 2,696 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,696 in last 12 months

Showing 2042120440 of 53,621 recalls

Medical DeviceMarch 23, 2020· Janus Trade Group

Recalled Item: B. Braun Introcan Safety IV Catheters Recalled by Janus Trade Group Due to...

The Issue: Distribution of B.Braun Introcan Safety IV catheters without a 510(k) within...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· INARI MEDICAL

Recalled Item: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/...

The Issue: The hemostasis valve of aspiration guide catheter devices may fail to seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· Abbott Diagnostics Technologies AS

Recalled Item: Power supply provided with Afinion 2 Recalled by Abbott Diagnostics...

The Issue: The analyzer system may have an electrostatic discharge and sparking of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· The Magstim Company Limited

Recalled Item: Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is Recalled...

The Issue: It was identified that there is a potential for the Stim Interconnecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· The Magstim Company Limited

Recalled Item: Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for...

The Issue: It was identified that there is a potential for the Stim Interconnecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...

The Issue: There was no data to validate that the identified endo-therapy devices were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Pleuravideoscope Recalled by Olympus Corporation of the Americas Due...

The Issue: There was no data to validate that the identified endo-therapy devices were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre 5F Plus Over the Wire Embolectomy Catheter Recalled by LeMaitre...

The Issue: There has been an increased trend in reports of catheters failing to deflate...

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

Class I — Serious Health HazardOngoing
FoodMarch 20, 2020· Winter Gardens Quality Foods, Inc.

Recalled Item: Whole Foods Vodka Sauce Recalled by Winter Gardens Quality Foods, Inc. Due...

The Issue: The product is being recalled for undeclared allergen (Milk).

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 20, 2020· Tiffany Food Corp.

Recalled Item: HUANGFUSHANZHEN Recalled by Tiffany Food Corp. Due to Undeclared Sulfites

The Issue: Product contains undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 20, 2020· Utak Laboratories Inc

Recalled Item: Utak NR Trace Elements Serum Control Recalled by Utak Laboratories Inc Due...

The Issue: The product has an incorrect value for cadmium and an incorrect expected range.

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

Class III — Low RiskOngoing
Medical DeviceMarch 20, 2020· Physio-Control, Inc.

Recalled Item: LifePAK 500 Automated External Defibrillator Recalled by Physio-Control,...

The Issue: Automated External Defibrillators may not detect a patient connection due to...

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2020· Edge Pharma, LLC

Recalled Item: Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free...

The Issue: Lack of Assurance of Sterility; the media used to conduct post-compounding...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2020· Edge Pharma, LLC

Recalled Item: Methotrexate Recalled by Edge Pharma, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; the media used to conduct post-compounding...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2020· Filltech USA, LLC

Recalled Item: Dermatone (avobenzone Recalled by Filltech USA, LLC Due to Microbial...

The Issue: Microbial contamination of non-sterile products: positive test for yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2020· Filltech USA, LLC

Recalled Item: Dermatone (avobenzone Recalled by Filltech USA, LLC Due to Microbial...

The Issue: Microbial contamination of non-sterile products: positive test for yeast and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2020· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension Recalled by PAI Holdings, LLC. dba Pharmaceutical...

The Issue: SubPotent Drug: Low out-of-specification results for assay testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc. Due to CGMP...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund