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. 2,820 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,820 in last 12 months

Showing 81618180 of 13,536 recalls

DrugMarch 17, 2017· Shire

Recalled Item: Kalbitor (ecallantide) Recalled by Shire Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Cream UPS Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: Certain lots of Fluocinonide Cream...

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2017· Akorn, Inc.

Recalled Item: LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of...

The Issue: Lack of assurance of sterility: product was found to be empty, under-filled,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2017· Allergan Sales, LLC

Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01% Recalled by Allergan Sales,...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 16, 2017· Fresenius Kabi USA, LLC

Recalled Item: Fluphenazine Decanoate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...

The Issue: Failed Dissolution Specifications; 9 month long term stability

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2017· Akorn Inc

Recalled Item: Sulfamethoxazole and Trimethoprim Oral Suspension Recalled by Akorn Inc Due...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2017· Genentech Inc.

Recalled Item: Cotellic (cobimetinib) Tablets Recalled by Genentech Inc. Due to Superpotent...

The Issue: Superpotent Drug: An oversized tablet was found in a bottle.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian...

The Issue: Defective Delivery System; reports of the device failing to activate which...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg Recalled by Meridian...

The Issue: Defective Delivery System; reports of the device failing to activate which...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Fluconazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2017· Mckesson Medical Surgical

Recalled Item: hydrALAZINE HYDROCHLORIDE INJECTION Recalled by Mckesson Medical Surgical...

The Issue: Temperature Abuse: Certain pieces of these lots distributed by McKesson...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: STREE OVERLORD capsules Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: MAX MAN capsules Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: HARD TEN DAYS capsules Recalled by A&H Focal Inc. Due to Marked Without An...

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found these products to...

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

Class II — Potential Health HazardOngoing
Refund