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. 2,841 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,841 in last 12 months

Showing 49214940 of 13,536 recalls

DrugDecember 4, 2019· American Health Packaging

Recalled Item: Raloxifene Hydrochloride Tablets Recalled by American Health Packaging Due...

The Issue: Failed Dissolution Specifications: Low out of specification results obtained...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2019· AuroMedics Pharma LLC

Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugDecember 2, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Amantadine Hydrochloride Tablets Recalled by Jubilant Cadista...

The Issue: Presence of Foreign Substance: Presence of a foreign object in a single tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2019· Pfizer Inc.

Recalled Item: 25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or expiration date.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals, LLC Due to Foreign...

The Issue: Presence of Foreign Substance: Foreign material found inside the vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....

The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2019· OraLabs, Incorporated

Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...

The Issue: Cross contamination with other products: undeclared contaminants of phenol...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· AuroMedics Pharma LLC

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Product complaints of discoloration after reconstitution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· Medisca, Inc.

Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2019· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL Recalled by Pacira Pharmaceuticals, Inc. Due to Sub Potent Drug: Out...

The Issue: Sub Potent Drug: Out of Specification (OOS)

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· American Health Packaging

Recalled Item: Ranitidine Tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 19, 2019· AuroMedics Pharma LLC

Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...

The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2019· Akorn, Inc.

Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...

The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...

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

Class II — Potential Health HazardOngoing
Refund