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. 1,064 recalls have been distributed to North Carolina in the last 12 months.
Showing 16081–16100 of 54,363 recalls
Recalled Item: Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is Recalled by...
The Issue: Image acquisition failures and synchronization failure with the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer - Product Usage: Is a Recalled by...
The Issue: Image acquisition failures and synchronization failure with the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD Recalled by Medline...
The Issue: Potential for sterile barrier breach. Microscopic pinholes within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (IC-3893CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0 Recalled by...
The Issue: Due to a software defect that can intermittently cause the system to lock-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...
The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine 200mg Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...
The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bleomycin for Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Labeling: Not elsewhere classified: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avicel Recalled by DuPont Nutrition USA, Inc Due to Out of specification...
The Issue: Out of specification results for conductivity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: General Manual surgical instrument Recalled by M.D.L. S.r.l. Due to...
The Issue: Sterility assurance may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A300314A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspirated Cyto-Histological Biopsy needle Recalled by M.D.L. S.r.l. Due to...
The Issue: Sterility assurance may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog A303318A Recalled by C.R. Bard Inc Due to There is potential for...
The Issue: There is potential for packaging defects that may impact the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.