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.
Showing 5041–5060 of 13,536 recalls
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cool Mint Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Vaginal Inserts USP Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective Delivery System: complaints for difficulty in pushing the plunger...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Apotex Inc. Due to Presence of...
The Issue: Presence of Foreign Tablets/Capsules: a single tablet of Pravastatin 40 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 150 mg Distributed by: Chattem Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Zantac 150 mg Distributed by: Chattem Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cool Mint Tablets Maximum Strength Zantac 150 mg Sanofi Distributed by:...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals...
The Issue: Incorrect labeling: Incorrect or missing lot and/or exp date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prasugrel Tablets 5 mg Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Low out of specification dissolution results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.