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. 1,736 recalls have been distributed to North Dakota in the last 12 months.
Showing 40421–40440 of 47,938 recalls
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soliris (eculizumab) Recalled by Alexion Pharmaceuticals, Inc. Due to...
The Issue: Presence of Particulate Matter: Product failed the appearance for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package Recalled by...
The Issue: Printing error by the packaging manufacturer erroneously added a "GF" symbol...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...
The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...
The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...
The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR...
The Issue: Complaints were received that reported the stopcock of some Stopcock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE System Product Usage: The intended use of the device Recalled by...
The Issue: A bug in the software prevents the iGUIDE software from logging off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tytin Regular Set Recalled by Kerr Corporation Due to Kerr Corporation is...
The Issue: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ MOSAIQ is an oncology information system used to manage Recalled by...
The Issue: MOSAIQ does not re-calculate the agent volume when the user changes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.