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 2121–2140 of 47,938 recalls
Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orajel Baby Recalled by Church & Dwight Inc Due to Microbial Contamination...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZICAM COLD REMEDY MEDICATED NASAL SWABS Recalled by Church & Dwight Inc Due...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZICAM NASAL ALLCLEAR Recalled by Church & Dwight Inc Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...
The Issue: As a result of a comprehensive product performance review it was determine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bornstein Frozen Shrimp Meat Recalled by Bornstein Seafoods Inc Due to...
The Issue: The recall was the result of the firm's routine sampling program and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Recalled by DRG...
The Issue: An incoming complaint reported that the expiration date on the kit box label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...
The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.