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 25141–25160 of 28,688 recalls
Recalled Item: Restoris Multicompartmental Knee (MCK) System is an implant system designed...
The Issue: The product may be mislabeled and could result in the incorrect implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...
The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...
The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...
The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX RIS QDOC 5.8 Recalled by AGFA Corp. Due to Patient name displayed...
The Issue: Patient name displayed (printed) on the Patient Report was the wrong patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...
The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panaroma Central Station Product Usage: This device can view real time...
The Issue: Mindray has identified two issues with the Panorama Central Station. Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular...
The Issue: Defective component may cause extension sets to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...
The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...
The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Recalled by Roche...
The Issue: Numerous complaints have been filed that leaking cobas ¿ PCR media 4.3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atlantis PV Recalled by Boston Scientific Corporation Due to Reports of...
The Issue: Reports of physicians experiencing inability to pass a 0.035" guidewire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.