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. 1,091 recalls have been distributed to North Carolina in the last 12 months.
Showing 13681–13700 of 29,737 recalls
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: 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: 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: 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: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...
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: 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: 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: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...
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: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...
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: TransWarmer Warming Infant Transport Mattress Recalled by CooperSurgical,...
The Issue: The firm updated the IFU in April 2019 to clarify that use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN Recalled by...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.