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 28741–28760 of 29,496 recalls
Recalled Item: STERRAD NX Cassette Recalled by Advanced Sterilization Products Due to...
The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion EnVe Ventilator Designed for use on patients who require Recalled...
The Issue: CareFusion identified that the EnVe Ventilator may not hold the set Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand Arthroscope and Hardware Set Tray (sterilization tray)...
The Issue: The gravity steam, Ethylene Oxide (EO) and STERRAD 100S sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 220/240V. The Recalled by...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 100/120V. The Recalled by...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanta 2 Bed. The Advanta 2 Bed is intended for Recalled by Hill-Rom, Inc....
The Issue: During an evaluation of Advanta 2 siderail samples returned from the field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Stealth 360-degree Orbital Atherectomy Device (OAD) Recalled by...
The Issue: CSI has initiated a recall on specific lot numbers of Stealth 360-degree...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated...
The Issue: superDimension, Inc., is conducting a recall of certain superDimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS)...
The Issue: Synthes is initiating a Medical Device Labeling Correction following a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian Eclipse Treatment Planning System for radiotherapy...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning (for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe N Simple No-Sting Skin Barrier Film Recalled by Safe N Simple, LLC Due...
The Issue: The firm received a customer complaint of observed spots on the wipes. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.