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. 1,895 recalls have been distributed to North Carolina in the last 12 months.
Showing 27541–27560 of 29,737 recalls
Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...
The Issue: The firm is recalling these power cables due to a latent design reliability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...
The Issue: Complaints have been reported for brakes disengaging when the bed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....
The Issue: Synthes received a complaint from a customer in which the Hand Switch for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - Push...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity I.V. Start Kit Recalled by Covidien LLC Due to On March 26, 2013...
The Issue: On March 26, 2013 Covidien received a recall notice from one of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL DrySlide Oxidase Kit Recalled by Becton Dickinson & Co. Due to In-vitro...
The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier (ER320) Recalled by...
The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...
The Issue: Product coatings require 510K approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.