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. 2,816 recalls have been distributed to New Jersey in the last 12 months.
Showing 9581–9600 of 29,496 recalls
Recalled Item: The Hero Model 100 (H-100) is a system consisting of Recalled by Hero Health...
The Issue: Due to dispenser prompting for a missed dose that had already been dispensed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Prim CEM FXD BPLT 7 Recalled by Howmedica Osteonics Corp. Due to...
The Issue: The internal profile of the Triathlon Prim (Baseplate) is potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Arthroscopy Kit Recalled by Medline Industries Inc Due to The kits...
The Issue: The kits may contain an expired component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 ANTIGEN QC Recalled by Beckman Coulter Inc. Due to...
The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 ANTIGEN EXTRACTION SOLUTION Recalled by Beckman Coulter...
The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Knee Arthroscopy Kit Recalled by Medline Industries Inc Due to The...
The Issue: The kits may contain an expired component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to SARS-CoV-2...
The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Total Knee Recalled by Medline Industries Inc Due to The kits may...
The Issue: The kits may contain an expired component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Shoulder CDS convenience kits Recalled by Medline Industries Inc Due...
The Issue: The kits may contain an expired component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access SARS-CoV-2 Antigen Calibrators Recalled by Beckman Coulter Inc. Due...
The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Go Monitors Recalled by Verathon, Inc. Due to Handheld video...
The Issue: Handheld video monitor failed to meet the labeled IP67 rating which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to The accumulated dose...
The Issue: The accumulated dose is incorrectly displayed in certain situations. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to The accumulated dose is...
The Issue: The accumulated dose is incorrectly displayed in certain situations. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography Systems Revolution CT Recalled by GE Healthcare, LLC Due...
The Issue: The accumulated dose is incorrectly displayed in certain situations....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Models with SW version VD12 listed below: Artis zee Recalled by...
The Issue: Due to a software error, the IAS (Image Acquisition System) may sporadically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation...
The Issue: The screw cover at the tip of the probe may fall off after a cleaning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium Super Pulsed Laser System (TFL-PLS) & Pro Super Recalled by...
The Issue: Thermal injury following dusting and fragmenting treatment of ureteral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude SNAP Splittable Sheath Introducer Recalled by Merit Medical Systems,...
The Issue: There is a potential that 7F sheaths are packaged as 10F sheaths.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude SNAP Splittable Sheath Introducer Recalled by Merit Medical Systems,...
The Issue: There is a potential that 7F sheaths are packaged as 10F sheaths.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sharesource Connectivity Platform for Use with the Amia Automated PD System...
The Issue: Baxter Healthcare Corporation has identified that the AMIA Sharesource User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.