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 8001–8020 of 51,854 recalls
Recalled Item: HYDROmorphone in 0.9% Sodium Chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: rocuronium Recalled by Central Admixture Pharmacy Services Inc Due to Lack...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone in dextrose 5% Recalled by Central Admixture Pharmacy Services...
The Issue: Lack of assurance of sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3.1 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance Recalled by Philips North America Llc...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...
The Issue: When using affected curette and software, there is a discrepancy between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betaxolol Tablets Recalled by KVK-Tech, Inc. Due to Presence of Foreign...
The Issue: Presence of Foreign Tablets/Capsules: There is a potential presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile...
The Issue: Subpotent: Out of Specification result observed for Ketorolac assay levels,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.