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. 1,070 recalls have been distributed to South Carolina in the last 12 months.
Showing 13581–13600 of 51,854 recalls
Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item # 714-0706 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 743-0278 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 744-4875 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 731-0120 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 722-0105 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 721-0200 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 714-5000 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 744-4930 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 721-1000 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...
The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 12mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 10mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...
The Issue: Potential for patient data mismatch when using browser "back" button to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Standard PVC Laryngeal Masks Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The mask cuff may disconnect from the device's breathing tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-3C160: EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-1TQ180: EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.