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. 2,827 recalls have been distributed to New Jersey in the last 12 months.
Showing 6841–6860 of 29,496 recalls
Recalled Item: Quantum Perfusion Systems for CPB Recalled by Spectrum Medical Ltd. Due to...
The Issue: The ratchet and pawl had an out of tolerance geometry which exhibited as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System- For use in the in vitro quantitative Recalled...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVT Interface Module (PVT)-Laboratory Automation system Brand names of the...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Fluid ingress that can cause a loss of electrical funtion and failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Recalled by Alcon...
The Issue: Sterility; Steril surgical procedure packs contain incomplete seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR Recalled by DeVilbiss...
The Issue: The instruction manual is being replaced with an updated version that is in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody...
The Issue: Incorrect Number of Calibrator Levels (2) Set for the VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C50 1.1-intended for use in generating radiographic images...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...
The Issue: Due to potential software issue that may result in patient mix-up information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...
The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...
The Issue: Issue related to the operation of the arm latch within the column that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....
The Issue: Error in the Introduction section of the user manual that indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.