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. 1,003 recalls have been distributed to North Carolina in the last 12 months.
Showing 34481–34500 of 54,363 recalls
Recalled Item: 14cm QD Angle Attachment Product Usage: Product attachment Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRI AIR CONTROL Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMALL ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCC Soft Computer Softbank II software Product Usage: Supports single...
The Issue: Software error. Potential for incorrect results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bearing Sleeve Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRI SHORT ATTACHMENT Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 degree Contra Angle Attachment Product Usage: Pneumatic system Recalled...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Softbank software Product Usage: Decision support software for transfusion...
The Issue: Software error. Potential for incorrect results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot control irrigation system Product Usage: Pneumatic system Recalled by...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 19cm Attachment Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III with Foot Guard Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11.0cm Long Attachment Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III with Irrigation Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0cm Short Attachment Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB101218...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C70¿ S61CM D66CM Catalog # AB081041 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB10218 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C90¿ S79CM D84CM Catalog # AB081046 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.