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. 2,654 recalls have been distributed to South Carolina in the last 12 months.
Showing 14221–14240 of 28,688 recalls
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth...
The Issue: An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece...
The Issue: Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Solstice(TM) SRS Immobilization System Recalled by Med Tec Inc Due to...
The Issue: There is a potential for movement of the Solstice Tilting Head Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Cuvette Segments Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Individual cuvettes within the Alinity c Cuvette Segment may become seated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD WAVELINQ 4F EndoAVF System Recalled by Bard Peripheral Vascular Inc Due...
The Issue: The firm has become aware of a potential problem with their venous and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posey Connected Twice-As-Tough Cuffs Recalled by TIDI PRODUCTS Due to Not...
The Issue: Not meeting design specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...
The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.