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. 2,553 recalls have been distributed to North Dakota in the last 12 months.
Showing 5221–5240 of 27,512 recalls
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed KIT Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Axillary Insertion Introducer -Introducer(s) are intended for...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The System is designed as a modular system with components Recalled by GE...
The Issue: GE HealthCare has become aware of the potential that incorrect torque has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Field Cric Kit with ET Tube Recalled by Sarnova HC, Llc Due to It...
The Issue: It was determined that the Endotracheal Tube Holder included in certain kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL:...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Pursue Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fountain Recalled by Merit Medical Systems, Inc. Due to The sterility of...
The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A Recalled by...
The Issue: Reports of a pink or green coloration of the image. If the issue is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Cricothyrotomy Field Kit with Instruments Recalled by Sarnova HC,...
The Issue: It was determined that the Endotracheal Tube Holder included in certain kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator Recalled...
The Issue: AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon...
The Issue: Certain factory settings for the device were incorrectly described in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride: Product Name/Product Code: 10ML IV FLUSH STERILE...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Water/Saline: Product Name/Product Code: CUP STERILE WATER¿ FOIL LID...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.