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. 2,108 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,108 in last 12 months

Showing 73817400 of 53,621 recalls

Medical DeviceDecember 28, 2023· MRP, LLC dba Aquabiliti

Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...

The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2023· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is expanding their previous product correction actions to a...

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

Class I — Serious Health HazardOngoing
DrugDecember 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...

The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL)...

The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL)...

The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...

The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose...

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: New warnings are being added to the Instructions for Use for all affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: IFU has been updated to include warnings about the risk of the inlet...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 26, 2023· Ossur H / F

Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...

The Issue: Knee batteries may need replacement with conforming batteries to ensure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· GE Medical Systems, SCS

Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...

The Issue: X-ray exposure termination audible signal on Senographe Pristina with...

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

Class II — Potential Health HazardOngoing
DrugDecember 26, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Amneal...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 26, 2023· Amerisource Health Services LLC

Recalled Item: Benzonatate Capsules Recalled by Amerisource Health Services LLC Due to...

The Issue: Superpotent drug: Assay results were slightly above specification at the...

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

Class III — Low RiskOngoing
Refund
DrugDecember 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund