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. 1,061 recalls have been distributed to North Dakota in the last 12 months.
Showing 8601–8620 of 47,938 recalls
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Magill Recalled by TELEFLEX LLC Due to Reports...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCHELIT Safety Clear Tracheal Tube Recalled by TELEFLEX LLC Due to Reports...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Travoprost Ophthalmic Solution Recalled by Golden State Medical Supply Inc....
The Issue: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NeuMoDx Cartridge-used for extraction Recalled by NeuMoDx Molecular Inc Due...
The Issue: Top label on some of the NeuMoDx cartridges within these lots may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.