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. 992 recalls have been distributed to North Dakota in the last 12 months.
Showing 19001–19020 of 47,938 recalls
Recalled Item: Hydroxocobalamin Injection Recalled by Fusion IV Pharmaceuticals, Inc. dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hungry Root Dairy free Garlic Parm sauce Recalled by The Honest Stand Due to...
The Issue: Undeclared Allergen: Product contains both cashews and almonds, but only...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 Recalled by...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CHEM8+ cartridges (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 3mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth...
The Issue: The catheter locks for the lot may contain an 8Fr catheter lock instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Bluntfill with Filter Recalled by Cardinal Health 200, LLC Due to...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 Recalled by...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to Recalled by...
The Issue: Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT G3+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: Marketed without a 510(k). Abbott Point of Care has determined that it does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Recalled by...
The Issue: The filter installed onto the tube set may have the incorrect pore size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Simulus 750 Flexible Ring/Band Accessory Kit - Product Usage:...
The Issue: Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...
The Issue: Subpotent: Out of specification for assay at the 12-month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: methylPREDNISolone Sodium Succinate For Injection Recalled by Hikma...
The Issue: Labeling: Incorrect Instructions: Vial label incorrectly instructs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ormco Damon Q2 Orthodontic Metal Bracket Recalled by Ormco/Sybronendo Due to...
The Issue: The bracket torque was mislabeled on the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telescopic Smoke Evac Pencil Recalled by Stryker Instruments Div. of Stryker...
The Issue: Hairline fractures in a component could allow electrical current to arc out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Recalled by...
The Issue: Incorrect power of lenses than the expected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeAir Telescopic Smoke Evacuation Pencil Recalled by Stryker Instruments...
The Issue: Hairline fractures in a component could allow electrical current to arc out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DP-30 Digital Ultrasonic Diagnostic Imaging System Recalled by Mindray DS...
The Issue: The DP-30 displays an incorrect needle-guide bracket when used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.