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. 2,723 recalls have been distributed to South Carolina in the last 12 months.
Showing 4641–4660 of 28,688 recalls
Recalled Item: SYRINGE Recalled by Alcon Research, LLC Due to Medline Bulb irrigation...
The Issue: Medline Bulb irrigation syringes recalled due to potential for packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nimbus II Infusion System Recalled by InfuTronix LLC Due to InfuTronix is...
The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Tube Securement Device Recalled by 3M Company - Health Care Business Due...
The Issue: Manufacturing nonconformities are in some lots of the Tube Securement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALYARD SURGICAL HOOD Recalled by O&M HALYARD, INC. Due to Mislabeling
The Issue: Product was mislabeled as a Surgical Cap at its dispenser level.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific iSLEEVE EXPANDABLE Introducer Set Recalled by Boston...
The Issue: Boston Scientific is conducting a removal of specific batches of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kits that include High Crack Check Valve PN...
The Issue: Pressure relief valve included in certain lots of cardiovascular procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Recalled...
The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Recalled...
The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec EsteemBody Soft Convex Recalled by ConvaTec, Inc Due to Convatec...
The Issue: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single...
The Issue: A deterioration of the cutting knife, including overheating and burning, can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus...
The Issue: A deterioration of the cutting knife, including overheating and burning, can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Ten 10ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abre Venous Self-expanding Stent System Recalled by Medtronic Inc. Due to...
The Issue: There is a potential for sterile package breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.