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. 2,757 recalls have been distributed to New Jersey in the last 12 months.
Showing 15061–15080 of 29,496 recalls
Recalled Item: MR-OR 1.5T Recalled by Philips Medical Systems Nederlands Due to There is a...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T for PET Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 0.5T Standard Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Anesthesia WT(P) 180 Recalled by Draeger Medical, Inc. Due to...
The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 5000 Series Washer/Disinfector Model # 5052 Recalled by Steris...
The Issue: The software in the systems may not process the cycle originally intended....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 3000 Series Washer/Disinfector Model # 3052 Recalled by Steris...
The Issue: The software in the systems may not process the cycle originally intended....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AST Indicator Recalled by Becton Dickinson & Co. Due to Panels...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AP AST Indicator Bag Recalled by Becton Dickinson & Co. Due to...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AST-s Indicator Recalled by Becton Dickinson & Co. Due to Panels...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.