Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,363 recalls have been distributed to North Dakota in the last 12 months.
Showing 25481–25500 of 27,512 recalls
Recalled Item: 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an Recalled by Ziemer Usa...
The Issue: A defect in the controller board can lead to the condenser to the video...
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: 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: 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: 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: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...
The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...
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: 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: 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: Various types of Fetal Bovine Serum Bovine sourced Animal Sera Recalled by...
The Issue: Current product labeling band data sheets state that FBS Pharma Grade and...
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: Curity Staple Remover 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: 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: BBL DrySlide PYR 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: 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.