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. 1,116 recalls have been distributed to Georgia in the last 12 months.
Showing 14841–14860 of 29,505 recalls
Recalled Item: Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape...
The Issue: The device label incorrectly states that the device is sterile. This product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL RuSCH One piece Male External Medium Catheter W/O Tape...
The Issue: The device label incorrectly states that the device is sterile. This product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: icumedical Oncology Kit w/12" Ext Set w/Spiros w/Red Cap Recalled by ICU...
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.
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.