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. 2,415 recalls have been distributed to North Dakota in the last 12 months.
Showing 18281–18300 of 27,512 recalls
Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...
The Issue: Endologix updated information on the rates of Type III endoleaks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issue on strain categorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Radial Head Prosthesis System Recalled by Synthes (USA) Products LLC...
The Issue: There is the possibility that the radial stem may loosen post-operatively at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.