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. 2,753 recalls have been distributed to New Jersey in the last 12 months.
Showing 15541–15560 of 29,496 recalls
Recalled Item: Solar 8000i Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuoSaph Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: The system's IFU contains a list of generators that the have been deemed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...
The Issue: the Ball Cube II phantom calibration film was not manufactured within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB + Multi-Lumen CVC Kit Recalled by Arrow International Inc Due to...
The Issue: The product was shipped after its expiry date due to a system error. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitek Screw and Washer Depth Gauge Recalled by DePuy Mitek, Inc., a Johnson...
The Issue: The device has an offset in the design that results in a reading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 2nd Edition Imaging System Recalled by Medtronic Navigation,...
The Issue: Software anomalies were reported to affect the following system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT cSystems ICT Module Recalled by Abbott Laboratories, Inc...
The Issue: There is a potential to generate falsely elevated serum or plasma chloride...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2 Recalled by...
The Issue: The reagent pack exhibits the potential for an increased frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Hexapod Strut Recalled by Stryker GmbH Due to The press fit...
The Issue: The press fit connection of the Angular Sleeve and pin of the U-Joint and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.