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 4981–5000 of 28,688 recalls
Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...
The Issue: The jaw may fracture prior to the procedure during the inspection instructed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel Plus (Pneumoplus) Recalled by BioFire Diagnostics,...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiaSorin LIAISON HSV-2 Type Specific IgG Recalled by Diasorin Inc. Due to...
The Issue: DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails: Software Version 5.1.0.X Recalled by PHILIPS MEDICAL...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500: Software Version 5.0 Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate Recalled by Greiner...
The Issue: Tubes have missing additive/anticoagulant resulting in clotting in most...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion system Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: System may exhibit a loss of imaging functionality and data due to an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to Potential...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill Recalled by Globus Medical, Inc. Due to...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C20 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill with Stop Recalled by Globus Medical, Inc. Due...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to Potential...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill with Stop Recalled by Globus Medical, Inc. Due...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.