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. 2,701 recalls have been distributed to South Carolina in the last 12 months.
Showing 9801–9820 of 28,688 recalls
Recalled Item: DIALYSIS ACCESS Medical convenience kit Recalled by Avid Medical, Inc. Due...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 3T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Recalled by INNOVA...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT CHEST TUBE TRAY. Medical convenience kit Recalled by Avid Medical,...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 7T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 Recalled by...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture. MAI Kit Part Number: 80315D Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Midline Insertion DA. MAI Kit Part Number: 77981B Recalled by Medical...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Injection REVIEW MAI Kit Part Number: 74736 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture MAI Kit Part Number: 80076 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tripolar Hooked Stimulation Probes Recalled by Spes Medica Due to The...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SNS Disposable Urethral Catheter Electrode Recalled by Spes Medica Due to...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly Laryngeal Surface Electrode Recalled by Spes Medica Due to The...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SNS Disposable Urethral Catheter Electrode Recalled by Spes Medica Due to...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly Laryngeal Surface Electrode Recalled by Spes Medica Due to The...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.