Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,997 recalls have been distributed to North Carolina in the last 12 months.
Showing 13661–13680 of 29,737 recalls
Recalled Item: Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage:...
The Issue: Negative Bias with Lot EA9227.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Cogent Hemodynamic Monitoring System Recalled by ICU Medical,...
The Issue: Firm identified several software issues through internal testing of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom Receiver Recalled by Dexcom Inc Due to It has been reported that use...
The Issue: It has been reported that use of the mobile receiver with software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an in vitro diagnostic product intended for use Recalled by Randox...
The Issue: Randox Laboratories realigned RX Analyser Series calibration targets by 10%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Pelvic Trainer (MPT) Recalled by Ralston Group Due to The device was...
The Issue: The device was incorrectly listed with the FDA and is therefore considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number...
The Issue: The sets are configured with quick connectors that have been assembled in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.