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 1936119380 of 28,688 recalls

Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: A problem can occur with the small light marker windows, used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes....

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Ultroid Technologies, Inc.

Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...

The Issue: Products are not designed, qualified, manufactured, and/or managed under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...

The Issue: Hardware issue that may expose the user to a potential risk for serious...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2016· Teleflex Medical

Recalled Item: Sheridan/CF Recalled by Teleflex Medical Due to Labeling inconsistency -...

The Issue: Labeling inconsistency - units labeled with a 7mm tube may contain a size...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2016· Spacelabs Healthcare Inc

Recalled Item: Xhibit Central Station Recalled by Spacelabs Healthcare Inc Due to The firm...

The Issue: The firm received reports of telemetry SpO2 numerics dropping off the Xhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Covidien LLC

Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...

The Issue: Sterility of the outer surface of the container compromised due to packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Reshape Medical Inc

Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...

The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance ICT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 12, 2016· Bausch & Lomb, Inc.

Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...

The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...

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

Class II — Potential Health HazardOngoing