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 24981–25000 of 28,688 recalls
Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...
The Issue: Labeling discrepancy.The label states that the implantable port contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...
The Issue: On a rare occasion the D-10 software might generate an extra result by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475625 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety glasses made with "Rage" frames manufactured between February 20...
The Issue: Fifteen pairs of prescription, safety glasses did not meet required,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOST Options" System (MOST) HINGED TIB INS SZ 1 16MM Recalled by Zimmer,...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo" Knee System: APOLLO PATELLA SZ0 28MM R Recalled by Zimmer, Inc. Due...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo" Knee System: PS TIB INS SZ0/16MM APOLL PS TIB Recalled by Zimmer,...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II System: POLY ULTRA TIB LT SZ00/9M POLY ULTRA Recalled by...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo" Revision/Constrained Knee System: SZ0-16MM AK CCK TIB INSER SZ1-11MM...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II System ULTRA CONG INS LT SZA/9MM ULTRA CONG Recalled by...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 Recalled by...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II Constrained Knee System NKII CCK TIB INS SZ00/0-L Recalled...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.