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. 1,061 recalls have been distributed to North Dakota in the last 12 months.
Showing 8361–8380 of 47,938 recalls
Recalled Item: Great Value Mixed Fruit. Pineppple Recalled by SunOpta Grains and Foods Inc....
The Issue: Fruit products have the potential to be contaminated with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good & Gather Mango Strawberry Blend. Whole Strawberries Recalled by SunOpta...
The Issue: Fruit products have the potential to be contaminated with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pineapple Chunks packaged under the following brand names and sizes....
The Issue: Fruit products have the potential to be contaminated with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mango Chunks packaged under the following brand names and sizes. Recalled by...
The Issue: Fruit products have the potential to be contaminated with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Whole Foods Market Organic Sliced Strawberries & Bananas. Net Recalled...
The Issue: Fruit products have the potential to be contaminated with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Whole Foods Market Organic Tropical Fruit Medley. Strawberries Recalled...
The Issue: Fruit products have the potential to be contaminated with Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lett Blend Rom/End/Rad - All Seasons Recalled by G.O. Corporation Due to...
The Issue: Romaine lettuce may be contaminated with deer feces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: A medical device correction is being issued for SIGMA Spectrum Infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE Suction Coagulators Recalled by Megadyne Medical Products, Inc. Due...
The Issue: An issue with the Suction Coagulator product family may lead to fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare Corporation Due...
The Issue: A medical device correction is being issued for SIGMA Spectrum Infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOLOMITE GLOSS ROLLATOR - intended to support during walking and Recalled by...
The Issue: Premature failure of the seat during use, the plastic eyelets of the folding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist intravascular micro axial blood pump Recalled...
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 2.5 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP with SmartAssist intravascular micro axial blood pump Recalled by...
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.0 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Direct Amplification Disc Kit Recalled by DiaSorin Molecular LLC...
The Issue: There is a potential for the direct amplification disc to malfunction which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella LD intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) Recalled by...
The Issue: Carryover from the Direct LDL-cholesterol assay on the Rx instruments may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2 Recalled...
The Issue: Dura regeneration matrix may have out-of-specification endotoxin levels due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.