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. 2,705 recalls have been distributed to South Carolina in the last 12 months.
Showing 7941–7960 of 28,688 recalls
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...
The Issue: Device was marketed without FDA 510(k) clearance or a PMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...
The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene CDF Nucleic Acid Test Recalled by Luminex Corporation Due to There...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER37000 programmer Model MER3400 software Recalled by St. Jude...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: There is a potential for programmer software (Merlin PCS) and remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin.net model MN5000 Software Recalled by St. Jude Medical, Cardiac...
The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...
The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS CoV 2 rapid antigen test kits packaged under the Recalled by North...
The Issue: Various brands of SARS CoV 2 Antigen Rapid Test kits were offered for sale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis with software version VD12A. A diagnostic and administrative tool...
The Issue: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe Combo with software version VD12A. A diagnostic and Recalled by...
The Issue: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Software Version 7.0 SP0.0.4.7 Recalled by GE Healthcare,...
The Issue: The Event Notification Manager (ENM) functionality for certain products does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO Recalled by SIGHT DIAGNOSTICS LTD Due to The default ranges for...
The Issue: The default ranges for MCH, MCHC, and RDW for age group "Child 2-11y" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative...
The Issue: The Instructions for Use (IFU, Part Number 750095) provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wright EVOLVE TRIAD Plate Cutter Recalled by Wright Medical Technology, Inc....
The Issue: The plate cutter is unable to meet sterilization requirements when it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeGlobal Fast Freeze Thawing Kit Recalled by CooperSurgical, Inc. Due to...
The Issue: There was translation error in the Spanish version of the IFU where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.