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. 928 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
928 in last 12 months

Showing 43761–43780 of 51,854 recalls

Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...

The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...

The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2014· Frito-Lay, Inc

Recalled Item: Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package Recalled by...

The Issue: Printing error by the packaging manufacturer erroneously added a "GF" symbol...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2014· Alexion Pharmaceuticals, Inc.

Recalled Item: Soliris (eculizumab) Recalled by Alexion Pharmaceuticals, Inc. Due to...

The Issue: Presence of Particulate Matter: Product failed the appearance for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 30, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...

The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...

The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...

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

Class III — Low RiskOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Carestream Health Inc.

Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...

The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Kerr Corporation

Recalled Item: Tytin Regular Set Recalled by Kerr Corporation Due to Kerr Corporation is...

The Issue: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Mckesson Medical Immaging

Recalled Item: Horizon Medical Imaging Horizon Medical Imaging is a medical image Recalled...

The Issue: Firm received a complaint that an unreported study performed that day could...

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

Class II — Potential Health HazardOngoing