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 25461–25480 of 27,512 recalls
Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Adult Manual Resuscitator Recalled by Carefusion 2200 Inc Due to...
The Issue: CareFusion has received four (4) customer reports of a component (oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HB1C Flex(R) Reagent Cartridge (DF105A Recalled by Siemens Healthcare...
The Issue: Positive bias on the lots listed compared to alternate methods and a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher & Paykel Healthcare ICON CPAP (continuous positive airway pressure)....
The Issue: Fisher and Paykel Healthcare is recalling the ICON CPAP units because there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HbA1c Flex(R) reagent cartridge (K3105A Recalled by Siemens Healthcare...
The Issue: Positive bias on the lots listed compared to alternate methods and a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24...
The Issue: Advanced Sterilization Products is recalling certain lots of STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brainlab Cranial Navigation System: An Image Guided Surgery System /...
The Issue: Software Error: The effect of setup on overall navigation accuracy could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...
The Issue: GE Healthcare has become aware of a potential data loss issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm Recalled by Cook,...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand OPMI Pentero C Recalled by Carl Zeiss Meditec, Inc. Due to Carl...
The Issue: Carl Zeiss Meditec is conducting a field corrective action for its OPMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Constellation Vision System Pneumatic Handpiece. Indicated for both...
The Issue: Alcon is conducting a Medical Device Removal for the Constellation Pneumatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LX System(s) and UniCel DxC 600/800 System(s) Lactate Reagent...
The Issue: Beckman Coulter initiated the recall for the Lactate Assay (LACT) Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...
The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The Recalled by...
The Issue: The firm initiated recall of Alere" hCG Combo Cassette (20/10 mIU/mL) kit PN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.