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. 1,836 recalls have been distributed to South Carolina in the last 12 months.
Showing 29621–29640 of 51,854 recalls
Recalled Item: Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specification: out of specification for tablet weight.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns Recalled by...
The Issue: Undeclared eggs
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AIRO Mobile CT System Recalled by Brainlab AG Due to Risk of unintended...
The Issue: Risk of unintended motion while the AIRO system is in transport mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter; stainless steel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...
The Issue: Presence of Particulate Matter: Silicone oil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acidophilus-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...
The Issue: Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Leci-thin-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared...
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Heart-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pancreas-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thymus Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: milk (Colostrum)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Liver-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: soy (lecithin)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metabo-Plus Recalled by NatureAll-STF Holding, LLC Due to Undeclared Allergens
The Issue: Undeclared allergens: milk (Whey)
Recommended Action: Do not consume. Return to store for a refund or discard.