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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 8721–8740 of 27,512 recalls
Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...
The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...
The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...
The Issue: Due to consoles not in compliance with the latest electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...
The Issue: It was noticed in production on 28.10.2021, that the final testing database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...
The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott HeartMate Touch Communication System Recalled by Thoratec Corp. Due...
The Issue: If LVAS communication system is trying to establish Bluetooth connection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iDesign Recalled by AMO Manufacturing USA, LLC Due to Aberrometer and...
The Issue: Aberrometer and precision laser systems are affected by a remote code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.