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. 2,793 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,793 in last 12 months

Showing 1142111440 of 29,505 recalls

Medical DeviceAugust 12, 2020· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...

The Issue: Connector between support surface and pump may be out of tolerance resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Encore Medical, LP

Recalled Item: RSP Standard HUMERAL SOCKET INSERT Recalled by Encore Medical, LP Due to...

The Issue: Product may be mislabeled with the size etched onto products differing from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Encore Medical, LP

Recalled Item: RSP Standard HUMERAL SOCKET INSERT Recalled by Encore Medical, LP Due to...

The Issue: Product may be mislabeled with the size etched onto products differing from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) Recalled by Maquet...

The Issue: Instruction For Use (IFU) incorrect serial number of 90437000. It should...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Boston Scientific Corporation

Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...

The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is...

The Issue: Potential sterility issue

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

Class II — Potential Health HazardOngoing