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. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 3121–3140 of 47,938 recalls
Recalled Item: Discovery XR656HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TISSUE APPROXIMATION SYSTEM (TAS) Recalled by TAS Medical Inc Due to Tissue...
The Issue: Tissue approximation straps (zip-ties) have broken before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH Recalled...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...
The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...
The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...
The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASIN B0CY2RDW5T Recalled by Amazon Retail LLC Due to Undeclared Egg
The Issue: Undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ASIN B084PZ7K98 Recalled by Amazon Retail LLC Due to Undeclared Egg
The Issue: Undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid...
The Issue: Devices were distributed in the U.S. market without obtaining the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device...
The Issue: Devices were distributed in the U.S. market without obtaining the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Module The BD Alaris System Recalled by CareFusion 303, Inc....
The Issue: Due to User Manual/Direction for Use incorrectly instructing user to leave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedFlex 2.0 Bio-ID Spare Parts by CareFusion 303, Inc. Due to Due...
The Issue: Due to fingerprint scanner failing resulting in the scanner heating up.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned Recalled by La Fiesta...
The Issue: Firm distributed a Seasoned Bread Crumb product with undeclared allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.