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. 2,837 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,837 in last 12 months

Showing 52015220 of 29,505 recalls

Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Truliant Knee System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Alteon Hip XLE Liner Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Logic Knee System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Novation Hip System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Vantage Ankle System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Logic PS Knee System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer running software version 1.16 or prior...

The Issue: There are potential performance issues found in the DxI 9000 Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Optetrak Knee System Recalled by Exactech, Inc. Due to Exactech has...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: AcuMatch Hip System Recalled by Exactech, Inc. Due to Exactech has received...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Equinoxe Shoulder System Recalled by Exactech, Inc. Due to Exactech...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Equinoxe Reverse Shoulder System Recalled by Exactech, Inc. Due to...

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Beckman Coulter, Inc.

Recalled Item: Access Ultrasensitive Insulin only used on the DxI 9000 Access Recalled by...

The Issue: There is an issue with the Access Ultrasensitive Insulin assay protocol file...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2023· Exactech, Inc.

Recalled Item: Exactech Vantage Mobile Bearing Tibial Inserts Recalled by Exactech, Inc....

The Issue: Exactech has received 3 complaints for 4 devices related to a loss of vacuum...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· ROi CPS LLC

Recalled Item: Regard Dressing change kit Recalled by ROi CPS LLC Due to ROi CPS...

The Issue: ROi CPS manufactured and distributed medical convenience kits with an...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 20, 2023· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS (PROCESSOR Recalled by LEICA BIOSYSTEMS NUSSLOCH...

The Issue: There is an issue regarding poorly processed and/or damaged biopsy tissue...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 - IVD For use as a Recalled by Randox Laboratories...

The Issue: Target for Alkaline Phosphatase (ALP) for the AMP optimized to IFCC 37¿C...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Randox Laboratories Ltd.

Recalled Item: Calibration Serum Level 3 CAL2351 Recalled by Randox Laboratories Ltd. Due...

The Issue: CK Total in Calibration Serum Level 3, CAL2351, is running with a positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Medtronic Inc.

Recalled Item: Protege GPS Self-Expanding Peripheral Stent System Recalled by Medtronic...

The Issue: Seal defects could compromise the ability of the product packaging to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2023· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model:...

The Issue: Instructions for Use-User Deviations related to the reprocessing of the...

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

Class II — Potential Health HazardOngoing