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. 2,529 recalls have been distributed to North Dakota in the last 12 months.
Showing 10561–10580 of 27,512 recalls
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...
The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Mg R1 - Product Usage: For the quantitative in Recalled by Randox...
The Issue: Failing to meet the linearity performance claims quoted on the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Rx Series Mg - Product Usage: For the quantitative Recalled by Randox...
The Issue: Failing to meet the linearity performance claims quoted on the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareLink Personal Software Therapy Management Software Tool for Diabetes...
The Issue: Incomplete basal rate information may be transmitted leading to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...
The Issue: A710 Intellis Clinician Application has a software issue that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Tip Guide- indicated for use in open Recalled by ConMed...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity ACL Tibial Elbow Guide-indicated for use in open and Recalled by...
The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling
The Issue: The product is mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life2000 Ventilation System Recalled by Hill-Rom Manufacturing, Inc. Due to...
The Issue: Under certain conditions, there is a risk for fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon PET-CT SCANNER Recalled by Canon Medical System, USA, INC. Due to A...
The Issue: A software problem has been identified which could result in the diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Adult Elongated O2/CO2 Mask - Product Usage: intended Recalled by Westmed,...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Elongated CO2/O2 Mask Recalled by Westmed, Inc. Due to There is a...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.