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. 2,639 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,639 in last 12 months

Showing 3292132940 of 53,621 recalls

DrugMarch 7, 2017· A&H Focal Inc.

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

Recalled Item: DADIYONGSHI XIANGGANGTIANLONGSHENGWU tablets Recalled by A&H Focal Inc. Due...

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: Miraculous Evil Root 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: Clalis capsules Recalled by A&H Focal Inc. Due to Marked Without An Approved...

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: GOLD VIGRA 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 I — Serious 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
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: 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 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: 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· 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: 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· 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· 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 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· 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· 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· 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