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. 2,572 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,572 in last 12 months

Showing 1950119520 of 28,688 recalls

Medical DeviceOctober 5, 2016· C.R. Bard, Inc.

Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....

The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...

The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...

The Issue: The device defect is a positive bias of up to 20% relative to the currently...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...

The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...

The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2016· Maquet Medical Systems USA

Recalled Item: Accessory Adapter Part number 600525A0 Product Usage: designed for the...

The Issue: Maquet Inc. is initiating a voluntary field action on the Accessory Adapter...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Medtronic

Recalled Item: Covidien Clearify Visualization System Item Code: 21-345 Intended to be...

The Issue: Product sterility is compromised due to breach of the sterile barrier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Nurse Assist, Inc

Recalled Item: Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe Recalled by...

The Issue: Potential contamination with B. cepacia.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 4, 2016· Medtronic

Recalled Item: Best Practices kits containing certain production lots of Clearify...

The Issue: Product sterility is compromised due to breach of the sterile barrier

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: COBAS INTEGRA 800 Tina-Quant Hemoglobin A1cDX Gen.2 Hemoglobin A1cDX test...

The Issue: .Roche Diagnostics has confirmed elevated QC and patient sample recovery for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant Hemoglobin A1c Gen. 2 Hemoglobin A1c test Catalog number Recalled...

The Issue: Roche Diagnostics has confirmed elevated QC and patient sample recovery for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Medtronic Neuromodulation

Recalled Item: Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is...

The Issue: Medtronic has identified an increased number of complaints from customers...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Implantable Drug Infusion System. This system...

The Issue: Medtronic is following up to a May 2013 communication regarding the Priming...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 3.0 mm Reaming Rod/950 mm Recalled by Synthes (USA) Products LLC Due to The...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm Recalled by Synthes (USA) Products...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Medimaps Group

Recalled Item: TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a Recalled by...

The Issue: The FRAX adjusted for TBS values are not correct when: The FRAX feature is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 2.5 mm Reaming Rod with Ball Tip & Extension/950 mm Recalled by Synthes...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 3.0 mm Reaming Rod/950 mm w/straight Ball Tip Recalled by Synthes (USA)...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: Extraction Hook - Sterile for TI Cannulated Nails Recalled by Synthes (USA)...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2016· Synthes (USA) Products LLC

Recalled Item: 3.0 mm Guide Rod/950 mm with Smooth Tip Recalled by Synthes (USA) Products...

The Issue: The peel pouches for the affected reaming rods and extraction hooks are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing