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. 2,671 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,671 in last 12 months

Showing 1322113240 of 28,688 recalls

Medical DeviceAugust 26, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...

The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2019· Ra Medical Systems, Inc.

Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...

The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2019· Philips North America, LLC

Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...

The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2019· LivaNova USA Inc

Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...

The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 22, 2019· Thoratec Switzerland GMBH

Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...

The Issue: Reports have been received of the CentriMag Systems experiencing motor and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: BALL NOSE GUIDE WIRE 80CM Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Hip systems Recalled by Zimmer Biomet, Inc. Due to Elevated levels...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: HA Pins (DFS HA Cort Screw) Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive RS Cleat CAP Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Recalled by...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: LT DISC ULNA - HA/PC Recalled by Zimmer Biomet, Inc. Due to Elevated levels...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: HENNESSY LEFT CONST GLENOID HA Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Various Custom Products Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Copeland HA Resurfacing Head Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: 2.0MM BALL NOSE GUIDE WIRE Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive HHR Tess Cleat Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2019· Zimmer Biomet, Inc.

Recalled Item: GUIDE WIRE 2.2MM X 28IN Recalled by Zimmer Biomet, Inc. Due to Elevated...

The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...

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

Class II — Potential Health HazardOngoing