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. 2,686 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,686 in last 12 months

Showing 2064120660 of 29,505 recalls

Medical DeviceJuly 1, 2016· Sysmex America Inc

Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...

The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Circulatory Technology Inc

Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...

The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...

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

Class III — Low RiskOngoing
Medical DeviceJuly 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...

The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Nidek Inc

Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...

The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· C.R. Bard, Inc.

Recalled Item: Medivance ArcticGel Neonatal Pad The pad is designed to fit Recalled by C.R....

The Issue: An internal review of an available product found that the Information For...

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

Class III — Low RiskOngoing
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Gmbh

Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...

The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· C.R. Bard, Inc.

Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem

The Issue: Labeling problem

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Select Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Trividia Health

Recalled Item: TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with Recalled...

The Issue: Product gives incorrect low blood glucose levels.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess...

The Issue: It was reported that the specified lots of the 2.4mm Titanium Locking Screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· CHG Hospital Beds Inc

Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...

The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2016· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to Wire in...

The Issue: Wire in tubing can become exposed, posing potential harm to the intubated...

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

Class II — Potential Health HazardOngoing