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. 2,652 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,652 in last 12 months

Showing 1452114540 of 28,688 recalls

Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: MultiDiagnost Eleva w/ Flat Detector Recalled by Philips North America, LLC...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: URODiagnost Eleva Recalled by Philips North America, LLC Due to The locking...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2019· Philips North America, LLC

Recalled Item: Urodiagnost Recalled by Philips North America, LLC Due to The locking plate...

The Issue: The locking plate may be missing from the system, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2019· Brainlab AG

Recalled Item: Spine & Trauma 3D Navigation 1.0 (subpart of the system Recalled by Brainlab...

The Issue: In certain occurrences, the affected navigation software application might...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 27, 2019· Cypress Medical Products LLC

Recalled Item: McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test Recalled...

The Issue: Products were denied Clinical Laboratory Improvement Amendments (CLIA)...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Biomet 3i, LLC

Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...

The Issue: During manufacturing, the screw stop ledge was not made to specification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Abbott Gmbh & Co. KG

Recalled Item: Abbott Alinity c Processing Module LN 03R67-01 - Product Usage: Recalled by...

The Issue: The safety interlock covering the septum piercing probes within the bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2019· Abbott Gmbh & Co. KG

Recalled Item: Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: Recalled by...

The Issue: The safety interlock covering the septum piercing probes within the bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2019· Nidek, Inc.

Recalled Item: NIDEK Specular Microscope Recalled by Nidek, Inc. Due to The electromagnetic...

The Issue: The electromagnetic noise exceeded the upper limit of the Electromagnetic...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach Recalled...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach Recalled...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Jugular Vein Approach Recalled by...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 22, 2019· Keystone Dental Inc

Recalled Item: Paltop Fully Guided Surgical Kit- containing the 1.25mm Hex Driver Recalled...

The Issue: Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly...

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

Class II — Potential Health HazardOngoing