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. 2,766 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,766 in last 12 months

Showing 1476114780 of 29,505 recalls

Medical DeviceMarch 13, 2019· Vyaire Medical

Recalled Item: enFlow Disposable Cartridge Recalled by Vyaire Medical Due to Testing has...

The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2019· Vyaire Medical

Recalled Item: enFlow Disposable Cartridge with IV Extension Set Recalled by Vyaire Medical...

The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Covidien Endo Clinch II Auto Suture Grasper Recalled by COVIDIEN LLC Due to...

The Issue: Sterilization method used was not consistent with the labeling and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...

The Issue: Sterilization method used was not consistent with the labeling and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Procedure kits include devices from the affected lots distributed OUS...

The Issue: Sterilization method used was not consistent with the labeling and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Exactech, Inc.

Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...

The Issue: 2.5 Truliant Fit Trays were mismarked as 3

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits Recalled...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL Recalled by...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM)...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Elekta Limited

Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...

The Issue: Users need to be aware when using these protocols for daily on line plan...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Beaver Visitec

Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling

The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...

The Issue: One of the software algorithms used to detect sample dispense errors was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Brainlab AG

Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...

The Issue: There is a potential for an incorrect dose distribution calculation by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Salto Talaris Tibial Ankle Prosthesis Tray Recalled by Integra LifeSciences...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades:Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing