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. 1,171 recalls have been distributed to New Jersey in the last 12 months.
Showing 921–940 of 29,496 recalls
Recalled Item: Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400...
The Issue: Instructions for use for a foot plating system is being updated to remove...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...
The Issue: When appending a care plan that contains one or more wave medication orders,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...
The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) Recalled...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number:...
The Issue: Due to two distinct issues: 1. During patient admission, patient demographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuRgical Planner (SRP) Recalled by Surgical Theater Inc Due to A software...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP)...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalyft PL & PL40 Expandable Interbody System labeled as follows Recalled...
The Issue: Expandable interbody system cage may loose height or collapse (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Navigation Advanced Platform (SNAP) Recalled by Surgical Theater...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) labeled as the following with...
The Issue: Potential for Automated Impella Controller (AIC) purge pressure issues due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Planner Recalled by Surgical Theater Inc Due to A software anomaly,...
The Issue: A software anomaly, under specific conditions when large rotational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number:...
The Issue: Due to Users not having access to the Instructions for Use/User Manual due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...
The Issue: Due to complaints of increased resistance when advancing the dilator within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.