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 28281–28300 of 29,496 recalls
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...
The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module System 9000 The Sarns Centrifugal...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: We are notifying you of a potential interaction between therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray V12 Size: 320 mm X 320 mm X 450 Recalled by Mindray DS USA, Inc....
The Issue: Mindray has identified an issue with the V Series Monitor where the monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01...
The Issue: The performance of the chemicals in the foam and vinyl are not consistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: An anomaly has been identified with the ARIA Oncology Information System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Centrifugal System Control module Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) received one report of loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The...
The Issue: Zimmer is initiating a lot specific recall of the NexGen¿ Stemmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...
The Issue: The Back Table Cover component in the custom pack was placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...
The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TM Ardis Interbody System Inserter Stainless Steel Recalled by Zimmer,...
The Issue: Zimmer Spine is has received complaints of difficulty in turning the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.