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. 2,753 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,753 in last 12 months

Showing 1518115200 of 29,505 recalls

Medical DeviceNovember 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Maximum Variable Pitch Compression Tray Base Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for silicone shedding during cleaning and sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2018· Howmedica Osteonics Corp.

Recalled Item: Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant....

The Issue: The surgical technique is being updated to caution against misuse due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· ICU Medical, Inc.

Recalled Item: ICU Medical Recalled by ICU Medical, Inc. Due to Reports of pressure tubing...

The Issue: Reports of pressure tubing separation between the sampling port and the high...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· ICU Medical, Inc.

Recalled Item: ICU Medical Recalled by ICU Medical, Inc. Due to Reports of pressure tubing...

The Issue: Reports of pressure tubing separation between the sampling port and the high...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· ICU Medical, Inc.

Recalled Item: ICU Medical Recalled by ICU Medical, Inc. Due to Reports of pressure tubing...

The Issue: Reports of pressure tubing separation between the sampling port and the high...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· Medtronic Perfusion Systems

Recalled Item: RESERVOIR "Y" ADAPTER Recalled by Medtronic Perfusion Systems Due to...

The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· Medtronic Perfusion Systems

Recalled Item: SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Recalled...

The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· AROA BIOSURGERY

Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...

The Issue: Potential for pouch seal failure

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· AROA BIOSURGERY

Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...

The Issue: Potential for pouch seal failure

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2018· AROA BIOSURGERY

Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...

The Issue: Potential for pouch seal failure

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2018· Smiths Medical ASD Inc.

Recalled Item: ProtectIV¿ Plus Safety IV Catheter Recalled by Smiths Medical ASD Inc. Due...

The Issue: Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2018· Philips North America LLC

Recalled Item: HeartStart MRx Recalled by Philips North America LLC Due to Affected...

The Issue: Affected lithium-ion batteries may contain a defective component (Thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Ferritin Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i TSH Reagent Kit Recalled by Abbott Ireland Diagnostics Division...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Progesterone Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Total Beta-hCG Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Estradiol Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i Free T4 Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2018· Abbott Ireland Diagnostics Division

Recalled Item: Alinity i 25-OH Vitamin D Reagent Kit Recalled by Abbott Ireland Diagnostics...

The Issue: Abbott has become aware of a manufacturing issue that can result in damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

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

Class II — Potential Health HazardOngoing