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. 2,743 recalls have been distributed to South Carolina in the last 12 months.
Showing 2201–2220 of 28,688 recalls
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paradigm insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog...
The Issue: Firm became aware of software issues related to most recent firmware update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...
The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Connected Blood Glucose Meter Recalled by Telcare, LLC Due to...
The Issue: Telcare, LLC has received customer complaints related to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...
The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Medical Video Upper GI Scope-Intended to provide optical...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Medical Video Colonoscope- Intended to provide optical visualization...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Processor- Intended to be used with PENTAX Recalled by...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker CinchLock Flex Knotless Anchor with Inserter and Suture Recalled by...
The Issue: Increase in complaints concerning "pullwire" breakage that may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR646 HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Definium 656HD & Discovery XR656HD (GTINs: 00840682138598 Recalled by GE...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery XR656 HD. X-Ray imaging system. Recalled by GE Medical Systems,...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery XR656HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.