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 16421–16440 of 29,737 recalls
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...
The Issue: If two devices are plugged into the same channel/port in the generator, both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS 5F DL XPP Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to A...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC (NV) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...
The Issue: Dental implants have incorrect item/lot numbers and size on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS TANDEM 5F DL BIOFLO PICC Recalled by Angiodynamics Inc. (Navilyst Medical...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Non-Valved with Nitinol GW PG Recalled by...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microintroducer Kit Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.