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. 2,529 recalls have been distributed to South Carolina in the last 12 months.
Showing 28081–28100 of 28,688 recalls
Recalled Item: Olympic Cool-Cap System is intended to provide treatment for neonatal...
The Issue: Olympic Cool-Cap Cooling Module's power supply failed during treatment. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II with swivel cable Product Codes Recalled by...
The Issue: MultiDiagnost Eleva X--Ray system may have damage to System Cables from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Formula Shaver Handpiece (with buttons) Recalled by Stryker Endoscopy Due to...
The Issue: Stryker Endoscopy determined that there may not have been adequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to software...
The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...
The Issue: An adverse trend of scale and bed exit service reports/complaints were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 4 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 2 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 8 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 13mm UPN Outer Box:...
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 11mm UPN Outer Box...
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.