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. 2,785 recalls have been distributed to Georgia in the last 12 months.
Showing 13721–13740 of 29,505 recalls
Recalled Item: CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186 Recalled by B....
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114 Recalled by B....
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187 Recalled by B....
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18TKSTN CONT EPID W/SOFT TIP NRFIT Catalog # 339191 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115 Recalled by B. Braun...
The Issue: The filter capacity is not achieved due to damage of the filter membrane.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer UDI:05700693930909 Recalled by Radiometer America Inc...
The Issue: Software Security; The action is being initiated because of software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis Commander Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis 8.3 Commander Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis 6.1 Commander Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lantis system (pre-2003) Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...
The Issue: code 7-102 Liquid Sensor Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...
The Issue: The action has been initiated to address reports of burst balloons which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...
The Issue: The action has been initiated to address reports of burst balloons which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.