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. 1,023 recalls have been distributed to New Jersey in the last 12 months.
Showing 32921–32940 of 53,621 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: ATENOLOL Tablets Recalled by Legacy Pharmaceutical Packaging LLC Due to...
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.
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.
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.
Recalled Item: Tiger King 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.
Recalled Item: Black Ant 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.
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.
Recalled Item: GERMANY BLACK GOLD tablets Recalled by A&H Focal Inc. Due to Marked Without...
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.
Recalled Item: Indian God Lotion Spray Bottle Recalled by A&H Focal Inc. Due to Marked...
The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HU HU SHENG WEI 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.