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 2584125860 of 28,688 recalls

Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S Recalled by Siemens Medical Solutions USA, Inc. Due to The...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia T Series SPECT + CT Product Usage 1) SPECT: Recalled by Siemens...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...

The Issue: The manufacturer has conducted a review of the results of product testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Steris Corporation

Recalled Item: Harmony Equipment Management System Recalled by Steris Corporation Due to...

The Issue: Dr¿ger Medical GmbH has notified STERIS of the potential for a break in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO - Beam shaping block for Radiation Therapy. Recalled by Elekta,...

The Issue: Clinical mistreatment may occur when there are errors in the clinical...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: STERILE SAMPLE BUILD Recalled by Medline Industries, Inc. Due to Guidewire...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Draeger Medical, Inc.

Recalled Item: Draeger Fabius GS Premium Recalled by Draeger Medical, Inc. Due to During...

The Issue: During final testing of the Draeger Fabius GS Premium, Fabius OS, and Fabius...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: ANGIOGRAPHY PACK Recalled by Medline Industries, Inc. Due to Guidewire...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: CATH LAB CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: ANGIO PACK #2 Recalled by Medline Industries, Inc. Due to Guidewire .035x150...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: CATH PACK Recalled by Medline Industries, Inc. Due to Guidewire .035x150...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: STERILE SAMPLE CATH LAB PACK Recalled by Medline Industries, Inc. Due to...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: STERILE SAMPLE BUILD Recalled by Medline Industries, Inc. Due to Guidewire...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: CATH PACK Recalled by Medline Industries, Inc. Due to Guidewire .035x150...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: CATH ANGIOGRAPHY DRAPE PACK Recalled by Medline Industries, Inc. Due to...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: CATH TRAY Recalled by Medline Industries, Inc. Due to Guidewire .035x150...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 14, 2013· Medline Industries, Inc.

Recalled Item: HEART CATH CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...

The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...

The Issue: Drug flow rates exceeding programmed flow rates.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2013· Ebi, Llc

Recalled Item: Cypher MIS Screw System Recalled by Ebi, Llc Due to Several complaints were...

The Issue: Several complaints were reported to exhibit screw head splay in the Cypher...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Kit (1 unit) Recalled by Codman & Shurtleff, Inc. Due to Drug flow...

The Issue: Drug flow rates exceeding programmed flow rates.

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

Class I — Serious Health HazardOngoing