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. 2,697 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,697 in last 12 months

Showing 1862118640 of 29,505 recalls

Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreathing Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Masks Recalled by ConvaTec, Inc Due to Reports of tubing detaching...

The Issue: Reports of tubing detaching from oxygen masks either prior to use (in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· Medtronic Navigation, Inc.

Recalled Item: Install CD Recalled by Medtronic Navigation, Inc. Due to Software issue...

The Issue: Software issue related to the StealthStation S7 system and the Synergy Spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Non-Rebreather Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Pediatric Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2017· ConvaTec, Inc

Recalled Item: Oxygen Mask Recalled by ConvaTec, Inc Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2)...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Covidien LLC

Recalled Item: Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: Recalled by...

The Issue: Cotton tip of the device may disengage due to insufficient adhesive

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arrow Multi-Lumen CVC Kit The Arrow Two-Lumen Central Venous Access Recalled...

The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Introducer Kit with Integral Hemostasis Valve/Side Port Recalled by Arrow...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended Recalled by...

The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing