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 26381–26400 of 28,688 recalls
Recalled Item: Stryker Instruments 0400-820-100 T5 Zipper Toga with Peel Away Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-100 T5 zipper Toga with Peel Away Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen...
The Issue: Failure to submit a premarket submission and gain approval of a medical device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments0400-750-000 T4 Toga Recalled by Stryker Instruments Div....
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-710-000 T4 Pullover Toga (S/M) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-000S2 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Radiation Therapy Treatment Planning System. Radiation...
The Issue: Patient needs to be positioned as indicated by the treatment plan.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches
The Issue: leaking pouches
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...
The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...
The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...
The Issue: There is a possibility that the pump head was not shipped in the locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....
The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...
The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Plus System The CoaguChek XS Plus system for Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.