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. 2,786 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,786 in last 12 months

Showing 1230112320 of 29,505 recalls

Medical DeviceApril 1, 2020· Aesculap Implant Systems LLC

Recalled Item: PRESTIGE RETRACTION GRASPER Recalled by Aesculap Implant Systems LLC Due to...

The Issue: Endoscopic graspers may become separated at the weld from handle to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2020· Aesculap Implant Systems LLC

Recalled Item: PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION Recalled by Aesculap Implant...

The Issue: Endoscopic graspers may become separated at the weld from handle to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CKMB Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The Spanish and Swedish language versions of the IFU state that the assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CKMB Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The Spanish and Swedish language versions of the IFU state that the assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2020· Spectranetics Corporation

Recalled Item: Bridge Occlusion Balloon Recalled by Spectranetics Corporation Due to There...

The Issue: There is a potential for thrombus formation on balloons prepped and staged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2020· Becton, Dickinson and Company, BD Biosciences

Recalled Item: Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US) Recalled by...

The Issue: False positive reaction on the reagent.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2020· Beckman Coulter Inc.

Recalled Item: iChem¿VELOCITY Urine Chemistry System- Recalled by Beckman Coulter Inc. Due...

The Issue: A defect in the SATA power adapter cable within the instruments computer has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2020· Beckman Coulter Inc.

Recalled Item: iQ200 Series Urine Microscopy Analyzer- All part numbers Recalled by Beckman...

The Issue: A defect in the SATA power adapter cable within the instrument s computer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2020· Boston Scientific Corporation

Recalled Item: MoXy Laser Fiber Recalled by Boston Scientific Corporation Due to To...

The Issue: To reinforce existing instructions within the Directions for Use (DFU) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2020· Elekta Inc

Recalled Item: Leksell Vantage Stereotactic System. Instrument Carrier Recalled by Elekta...

The Issue: A faulty locking piece of the Instrument Carrier that does not fulfil the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2020· Stryker Sustainability Solutions

Recalled Item: Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter Recalled by Stryker...

The Issue: A subset of temporary intracardiac ultrasound catheters are labeled with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2020· Edwards Lifesciences, LLC

Recalled Item: Sterile Oxymetry Oligon Catheter Kit. Pressure injectable....

The Issue: Sterile catheter kit packaging compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...

The Issue: In affected software version, of Positron emission tomography and computed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628...

The Issue: Nonconforming product; length of the product measured shorter than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel 2"x2" Saturated Gauze- A hydrating wound dressing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel 4"x8" Saturated Gauze- A hydrating wound dressing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel Hydrogel 4oz. Tube. Wound dressing containing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2020· Gentell, Inc

Recalled Item: Gentell Honey Hydrogel 4"x4" Saturated Gauze- A hydrating wound dressing...

The Issue: During an FDA audit, it was discovered that the product was not properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2020· Abbott Vascular

Recalled Item: Xience Sierra TM Everolimus Eluting Coronary Stent System Recalled by Abbott...

The Issue: Incorrect expiration date

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2020· INARI MEDICAL

Recalled Item: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/...

The Issue: The hemostasis valve of aspiration guide catheter devices may fail to seal...

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

Class II — Potential Health HazardOngoing