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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 27441–27460 of 29,496 recalls
Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...
The Issue: The firm is recalling the specific lot due to lower than expected results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...
The Issue: In rare instances, channel shifted results have been generated with cobas¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14212-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...
The Issue: The current Century Break patch did not contain the same setting for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...
The Issue: Correction to provide clarification and additional labeling to minimize...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking...
The Issue: Stryker Orthopaedics has received a report indicating that the scale of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMend¿ Extend" Absorbable Collagen Membrane BioMend¿ Extend" Absorbable...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTAT - Agent Recalled by Integra LifeSciences Corporation Due to Due to...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuraGen Nerve Guide NeuraGen Nerve Guide is indicated for repair Recalled...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MSK EXTREME MR SCANNER Recalled by GE Healthcare, LLC Due to Coolant supply...
The Issue: Coolant supply lines may leak liquid onto the floor resulting in a slippery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Layershield Adhesion Barrier Matrix Layershield Adhesion Barrier Matrix is...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR430s MRI Scanner Recalled by GE Healthcare, LLC Due to Coolant...
The Issue: Coolant supply lines may leak liquid onto the floor resulting in a slippery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.