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. 2,683 recalls have been distributed to New Jersey in the last 12 months.
Showing 21521–21540 of 29,496 recalls
Recalled Item: Brilliance iCT SP Computed Tomography X-ray Systems Recalled by Philips...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Stryker) AccuPlace Round Level Needle Guide Recalled by Stryker Instruments...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...
The Issue: The battery capacity of the optional PS500 power supply unit for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...
The Issue: During an evaluation of the product packaging, it was determined that there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion Tubing Pack Recalled by Medtronic Perfusion...
The Issue: Medtronic is notifying customers who have or may receive specific lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostic ADVIA Centaur Calibrator E- 6- Pack ()...
The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog...
The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...
The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MitraClip Clip Delivery System Recalled by Abbott Vascular Due to Abbott...
The Issue: Abbott Vascular has recently received reports of cases on Clip Delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...
The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...
The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...
The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Potential for RadSuite AV viewer to skip image slices when the user presses...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...
The Issue: Potential data loss occurs as a result of product archiving not working...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is an integrated Recalled...
The Issue: Patient information in the header is only found on the first page of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...
The Issue: The software was not presenting the PURE filter user interface message on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...
The Issue: A migrated study that has annotations will display the annotations, but when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...
The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.