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. 2,815 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,815 in last 12 months

Showing 97019720 of 29,505 recalls

Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Sunstar Americas, Inc.

Recalled Item: SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse Recalled by Sunstar Americas,...

The Issue: Products may be contaminated with micro-organisms Burkholderia cepacia...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2021· The Binding Site Group, Ltd.

Recalled Item: FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems Recalled...

The Issue: The high and low level "Quality Controls" demonstrate a positive bias of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost 4 High Performance. radiography and fluoroscopy system...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Philips Medical Systems DMC GmbH

Recalled Item: ProxiDiagnost N90. radiography and fluoroscopy system Recalled by Philips...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Philips Medical Systems DMC GmbH

Recalled Item: DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Recalled...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Recalled by...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing