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. 2,672 recalls have been distributed to South Carolina in the last 12 months.
Showing 11961–11980 of 28,688 recalls
Recalled Item: Cardiovascular Monitoring Device accessory - Product Usage: The chest...
The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.