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. 1,924 recalls have been distributed to North Carolina in the last 12 months.
Showing 21301–21320 of 29,737 recalls
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System PN: 989605858501 a whole Recalled by...
The Issue: The following issues are found in NeuViz 16 systems with software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...
The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...
The Issue: Incorrect expiration date was listed on the label. Correct expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...
The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics GBS Detect Cat no. A300. Used for the Recalled by Hardy...
The Issue: Performance failure; poor hemolytic reaction of non or weakly hemolytic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.