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. 955 recalls have been distributed to North Dakota in the last 12 months.
Showing 34761–34780 of 47,938 recalls
Recalled Item: Certain Micromini Flat Implant Cover Screw Dental implants Recalled by...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MECLIZINE HYDROCHLORIDE TABLETS Recalled by Golden State Medical Supply Inc....
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MECLIZINE HYDROCHLORIDE TABLETS Recalled by Golden State Medical Supply Inc....
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...
The Issue: Potential for separation of the proximal handle from the shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...
The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...
The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)...
The Issue: Mitek identified that on VAPR Tripolar 90 Degree Suction Electrode the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...
The Issue: "The public reason for the recall is that the product is being recalled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS Recalled by...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number:...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the...
The Issue: The firm discovered that information printed on the quick magnet is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve Recalled by Boston Scientific Corp...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 Recalled by Boston...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Made In Nature Sriracha Chili Kale Chips Recalled by Made In Nature, LLC Due...
The Issue: Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pacific Superfoods Snack Lava Rock Sriracha Kale Chips Recalled by Made In...
The Issue: Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.