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 98019820 of 29,505 recalls

Medical DeviceMay 5, 2021· Arcoma AB

Recalled Item: Omnera 400A Digital Radiographic System Recalled by Arcoma AB Due to There...

The Issue: There is the potential for the X-Ray system to short circuit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Arcoma AB

Recalled Item: Omnera 400T Digital Radiographic System Recalled by Arcoma AB Due to There...

The Issue: There is the potential for the X-Ray system to short circuit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: WorkMate Claris v.1.2 Upgrade Kits Recalled by Abbott Laboratories Inc. (St...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens...

The Issue: Photometer Lamp May Reach Saturation Without Flagging Results, may generate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: Recalled...

The Issue: Ortho investigated and confirmed the potential for unexpected failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing