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 27701–27720 of 29,496 recalls
Recalled Item: Helion S Exam Light or H300 The device is intended Recalled by Trumpf...
The Issue: Possible fatigue failure of the plastic joint may occur after an average use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...
The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...
The Issue: It was reported from a complaint that study category labels of "Prior" and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...
The Issue: A software defect was discovered that causes images to be out of context...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 and Ingenuity Computed Tomography X-Ray Systems The Brilliance...
The Issue: This field change order is being released to update software and customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...
The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...
The Issue: The bed frame adapter assemblies may have a weak weld where the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization Recalled...
The Issue: The control boards alarm set points and temperature tolerances allowed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.