Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,766 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,766 in last 12 months

Showing 1484114860 of 29,505 recalls

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· Luminex Molecular Diagnostics

Recalled Item: xTAG Gastrointestinal Pathogen Panel intended for the simultaneous...

The Issue: Reports have been received of lower MS2 MFI values when using the panel.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2019· GE Healthcare, LLC

Recalled Item: Integrated ECG cable with 3-lead leadwires labeled as the following:...

The Issue: The Integrated ECG cable with 3-lead leadwires can short circuit during...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 21, 2019· ArthroCare Corporation

Recalled Item: Smith&Nephew SmartStitch PerfectPasser Connector Recalled by ArthroCare...

The Issue: The voluntary recall is being initiated due to a manufacturing error...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoLock Closed Vial Spike w/Skirt Recalled by ICU Medical, Inc....

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing