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. 2,819 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,819 in last 12 months

Showing 71217140 of 29,505 recalls

Medical DeviceDecember 13, 2022· Olympus Corporation of the Americas

Recalled Item: SPiN Thoracic Navigation System Model: SYS-4000 (SYS-4000D) Recalled by...

The Issue: A grainy image is observed when using a SPiN Vision Single-Use Flexible...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc Host 2 as follows: Product SMN epoc Host 10736387 Recalled by Siemens...

The Issue: pO2 High Recovery in Quality Control When Adjusted for Barometric Pressure

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc Host 2 as follows: Product SMN epoc NXS Host Recalled by Siemens...

The Issue: pO2 High Recovery in Quality Control When Adjusted for Barometric Pressure

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Roche Diagnostics Operations, Inc.

Recalled Item: cobas infinity central lab Recalled by Roche Diagnostics Operations, Inc....

The Issue: A complaint investigation revealed that an incorrect behavior relating to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal ORGAN RECOVERY PACK PGYBK Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedBank System - Product Label/labeling pending Recalled by...

The Issue: Due to customer complaints related to the MedBank software which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Steam Test Pack (20 Tests and 20 controls) Item Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Steam Test Pack (20 Tests and 5 controls) Item Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing