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. 2,656 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,656 in last 12 months

Showing 2528125300 of 53,623 recalls

DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2018· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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
Medical DeviceNovember 19, 2018· Abbott

Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...

The Issue: The device is unable to pair with the mobile app due to the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2018· Arthrex, Inc.

Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...

The Issue: Potentially lead to anchor breakage during insertion,

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2018· Heartware, Inc.

Recalled Item: Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model...

The Issue: HVAD Battery Charger units manufactured with wrong inductors.

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

Class II — Potential Health HazardOngoing
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: SHEER DesenZ Desensitizing Treatment Recalled by CAO Group, Inc. Due to cGMP...

The Issue: cGMP violations noted during the firm's most recent inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: fas.TRACT Coagulative Hemostatic Gel Recalled by CAO Group, Inc. Due to cGMP...

The Issue: cGMP violations noted during the firm's most recent inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: FastStat Topical Hemostat Introductory Kit Recalled by CAO Group, Inc. Due...

The Issue: cGMP violations noted during the firm's most recent inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2018· CAO Group, Inc.

Recalled Item: BeeGentle Honey Flavored Topical Anesthetic Recalled by CAO Group, Inc. Due...

The Issue: cGMP violations noted during the firm's most recent inspection.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund