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. 2,859 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,859 in last 12 months

Showing 461480 of 29,505 recalls

Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sophysa

Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...

The Issue: Customer complaints of Pressio monitor rebooting.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sheathing Technologies Inc

Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...

The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Software version 5.10.1 and earlier contain anomalies that have the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...

The Issue: Potential for incomplete seal on header bag.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...

The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 13, 2025· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...

The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen App Recalled by Medtronic MiniMed, Inc. Due to When app is uninstalled...

The Issue: When app is uninstalled and reinstalled, insulin pen software issue causes...

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

Class II — Potential Health HazardOngoing