Product Recalls in South Carolina
Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,557 recalls have been distributed to South Carolina in the last 12 months.
Showing 21941–21960 of 28,688 recalls
Recalled Item: Philips Healthcare Brilliance iCT Computed Tomography X-Ray System Recalled...
The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System...
The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-Ray System Recalled...
The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-Ray System Recalled by...
The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-Ray System Recalled...
The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT SP Computed Tomography X-Ray System...
The Issue: Software Defects resulting in: (1) sagittal result shortened for axial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...
The Issue: There is a defect in one lot of a buffer, non-specific background staining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 123 POC system The cobas b 123 POC Recalled by Roche Diagnostics...
The Issue: under specific settings, an issue may occur during simultaneous Sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inserter for Titanium Elastic Nails (TEN) Recalled by Synthes (USA) Products...
The Issue: potential for mechanical failures such as breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 400 and AMSCO C Small Steam Sterilizers Recalled by Steris Corporation...
The Issue: In AMSCO Small Steam Sterilizers equipped with the CS-iQ feature, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer...
The Issue: In about 5% of tested samples, the outer tray was found to be compromised....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...
The Issue: The firm determined that 25 lots had been manufactured with a minor surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CryoConsole Recalled by Medtronic Inc. Cardiac Rhythm Disease...
The Issue: An issue with a USB memory component contained within a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Recalled by AGFA Healthcare Corp. Due to Customers have experienced...
The Issue: Customers have experienced IMPAX CV software, specifically, Demographics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.