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. 1,672 recalls have been distributed to North Dakota in the last 12 months.
Showing 41481–41500 of 47,938 recalls
Recalled Item: SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product...
The Issue: Baxter Healthcare Corporation has issued an Urgent Device Correction for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia and Infinia Hawkeye Nuclear Medicine Systems. For...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to Potential safety...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMP X-alt Acetabular Liner This acetabular liner is intended for Recalled by...
The Issue: Packaging error -- two different types and sizes of acetabular liners used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Grocers brand Dark Chocolate Almonds Recalled by Natural Grocers by...
The Issue: Natural Grocers by Vitamin Cottage is recalling one lot of six ounce...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gelnique (oxybutynin chloride) Gel 10% Recalled by Actavis Due to Subpotent...
The Issue: Subpotent Drug: Drug potency was compromised during shipment.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...
The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...
The Issue: Incorrect master label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Uncle Ben's (R) Recalled by Mars Food US Due to Reports of mild flushing...
The Issue: Reports of mild flushing reaction after consumption of product led to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...
The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...
The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...
The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...
The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.