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 82018220 of 13,536 recalls

DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended Release Tablets 30 mg Recalled by Alvogen,...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: Power V8 Viagra tablets 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 I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Pfizer Inc

Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...

The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Pfizer Inc

Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...

The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: ZHANSHENG WEIGE CHAOYUE XILISHI tablets Recalled by A&H Focal Inc. Due to...

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 I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: LIEN CHAN FOR SEVEN DAYS capsules Recalled by A&H Focal Inc. Due to Marked...

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 I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: MACA gold tablets 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 I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2017· A&H Focal Inc.

Recalled Item: GERMANY NIUBIAN tablets 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 I — Serious Health HazardOngoing
Refund
DrugMarch 6, 2017· GSK Consumer Healthcare

Recalled Item: Sensodyne Repair & Protect Whitening Recalled by GSK Consumer Healthcare Due...

The Issue: Presence of Foreign Substance; low concentration of an additional flavoring...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: RIVASTIGMINE Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Cross-contamination with other products -Related Substances test for...

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

Class III — Low RiskOngoing
Refund
DrugMarch 2, 2017· Fougera Pharmaceuticals Inc.

Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...

The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 1, 2017· Signature Club A Ltd

Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2017· G & W Laboratories, Inc.

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...

The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 24, 2017· Citron Pharma Llc

Recalled Item: Penicillin V Potassium Tablets Recalled by Citron Pharma Llc Due to Presence...

The Issue: Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 23, 2017· Mckesson Packaging Services

Recalled Item: Aspirin Chewable Tablets Recalled by Mckesson Packaging Services Due to...

The Issue: Presence of Foreign Substance: foreign material found in the bulk inventory.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2017· Endo Pharmaceuticals, Inc.

Recalled Item: Edex (alprostadil for injection) 10mcg Recalled by Endo Pharmaceuticals,...

The Issue: Lack of Assurance of Sterility: Defective container resulting in the lack of...

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

Class II — Potential Health HazardOngoing
Refund