Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,789 recalls have been distributed to North Carolina in the last 12 months.
Showing 7941–7960 of 29,737 recalls
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-150...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System with Version 3.7.2 and below Recalled by...
The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System with Version 3.7.2 and below Recalled by...
The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power electronic box Recalled by Myolyn Inc. Due to Screws mounting an...
The Issue: Screws mounting an internal power supply may come loose during shipping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Recalled by...
The Issue: Negative bias with patient samples. The mean patient sample bias range from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System...
The Issue: Incorrect expiration date listed on the product labels. The expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal limb holders: (1) DeRoyal Limb Holder Recalled by DeRoyal Industries...
The Issue: The webbing strap was laced improperly through the teeth of the buckle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Inaccurate Distance and Area measurements with use of Global Stack viewport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Ultrasound Systems (various models) used in conjunction with...
The Issue: Retroactive: Ultrasound may experience an unexpected automatic reboot,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Exacta-Mix 2400 compounding system Recalled by Baxter Healthcare...
The Issue: There is a potential for leaking valves on ports 1 to 4 in certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to SARS-CoV-2...
The Issue: SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier...
The Issue: Application error problems: Rebalance scope message: 1.Rebalancing process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e801 Immunoassay Analyzer Recalled by Roche Diagnostics Operations,...
The Issue: Software issue resulting in signals and sample test results of Pre-Wash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grappler Suture Anchor Recalled by Paragon 28, Inc. Due to Suture anchor may...
The Issue: Suture anchor may break upon insertion, which could lead to potential debris...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to...
The Issue: MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...
The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.