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.

51,854 total recalls
2,529 in last 12 months

Showing 2806128080 of 28,688 recalls

Medical DeviceMay 23, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...

The Issue: Philips is issuing a software update to the Intellispace Portal systems to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal software Product Usage: Intellispace Portal is a...

The Issue: In the Multi-Modality Tumor Tracking application, when changing the contours...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: TetraCXP Software System Recalled by Beckman Coulter Inc. Due to The recall...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: CYTO-STAT tetraCHROME CD45- FITC/CD56-RD1/CD19-ECD/CD3-PC5 Recalled by...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Beckman Coulter Inc.

Recalled Item: CYTO-STAT tetraCHROME CD45-FITC/CD4-RD1/CD8-ECD/CD3-PC5 Recalled by Beckman...

The Issue: The recall was initiated because Beckman Coulter has determined that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Philips Healthcare Inc.

Recalled Item: Philips Digital Diagnost Software Recalled by Philips Healthcare Inc. Due to...

The Issue: With Digital Diagnost (DIDI) R 2.0.2 a mirrored "R in a circle" is burnt...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm MRSA ACP Assay Catalog #441637 Recalled by Becton Dickinson & Co....

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm VanR Assay Recalled by Becton Dickinson & Co. Due to Leakage in...

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm MRSA ACP Assay Recalled by Becton Dickinson & Co. Due to Leakage...

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm Cdiff Assay Recalled by Becton Dickinson & Co. Due to Leakage in...

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Becton Dickinson & Co.

Recalled Item: BD GeneOhm Cdiff Assay Recalled by Becton Dickinson & Co. Due to Leakage in...

The Issue: Leakage in Cepheid SmartCycler reaction tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP PN 98000XR Intended to be used as Recalled by Alere San...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage Cardiac Panel PN 97000HS Used for the quantitative Recalled by...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage Profiler SOB Panel PN 97300 Used for the Recalled by Alere San...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Triage D-dimer PN 98100 Used as an aid in the Recalled by Alere San Diego,...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage CardioProfiler Panel PN 97100CP Used for the quantitative...

The Issue: Certain lots of the affected products may have significantly decreased...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2012· Synthes USA HQ, Inc.

Recalled Item: 4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 .019.038S...

The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2012· Synthes USA HQ, Inc.

Recalled Item: 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 .019.028S...

The Issue: Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Software For use in the in-vitro quantitative...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Software For use in the in-vitro quantitative...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing