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. 2,540 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,540 in last 12 months

Showing 2464124660 of 28,688 recalls

Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Ebi, Llc

Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...

The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...

The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Synthes, Inc.

Recalled Item: Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming...

The Issue: All lots of B37 Replacement Screws are being recalled due to potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...

The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific Chemistry Controls Level I and II LEVl: Amber Recalled by...

The Issue: The original mean assigned to the control too high, upon reassignment with...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2014· Beckman Coulter Inc.

Recalled Item: Ultrasonic Transducer Kits For use with the Access Family of Recalled by...

The Issue: Beckman Coulter is initiating a field action because some Ultrasonic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing