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. 2,862 recalls have been distributed to New Jersey in the last 12 months.
Showing 1381–1400 of 13,536 recalls
Recalled Item: Ranolazine Extended-Release Tablets 500mg Recalled by Glenmark...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Oral Suspension Recalled by The Harvard Drug Group LLC dba Major...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Deferasirox Tablets for Oral Suspension Recalled by Glenmark Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kuka Flex Forte caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxaydo (oxycodone HCl Recalled by Zyla Life Sciences US Inc. Due to...
The Issue: Sub-potent Drug: Lower potency than labeled.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Opium Tincture Recalled by Edenbridge Pharmaceuticals, LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Reumo Flex caplets Recalled by Botanical Be Due to Undeclared Diclofenac
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Origa y Omega 3 tablets Recalled by Botanical Be Due to...
The Issue: Marketed Without an Approved NDA/ANDA: products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%) Recalled by...
The Issue: CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam in 0.8% Sodium Chloride Injection 100 mg/100 mL (1mg/mL) Recalled...
The Issue: Presence of Particulate Matter: Silicone
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Presence of Particulate Matter: Silicone
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ELCYS (cysteine hydrochloride injection) Recalled by Exela Pharma Sciences...
The Issue: Presence of Particulate Matter: Silicone
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sucralfate Oral Suspension Recalled by VistaPharm LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminocaproic Acid Oral Solution Recalled by VistaPharm LLC Due to Failed...
The Issue: Failed Excipient Specifications: high content of ethylene glycol (EG)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.