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. 903 recalls have been distributed to South Carolina in the last 12 months.
Showing 50101–50120 of 51,854 recalls
Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/out Needles with Orthocord Product Number: 222969 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste...
The Issue: CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...
The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...
The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Inverse/Reverse Screw system Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Ball taper for humeral stem Recalled by Zimmer, Inc....
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DTO" Implant Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw Recalled by...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...
The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alloclassic SL Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿ screw ¿ 4.0 self-tapping Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile Recalled by...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox¿ Option Ceramic Femoral Head System Rx Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: zimmer Anatomical Shoulder Glenoid S Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.