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. 1,122 recalls have been distributed to North Dakota in the last 12 months.
Showing 441–460 of 47,938 recalls
Recalled Item: Medline medical procedure convenience kits labeled as: 1) ROBOTIC Recalled...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical TID Pharos Illuminated Depressor Recalled by Vortex Surgical...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecfen Retractable Membrane Polisher Recalled by Vortex Surgical Inc. Due to...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...
The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...
The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 25GA I.D.D. Internal Delivery Device Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE...
The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number:...
The Issue: The console label for affected devices is missing the "DANGER" symbol.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Precision IV Pump Recalled by ICU Medical, Inc. Due to...
The Issue: Plum Solo and Duo Infusion pumps include a feature, that when selected,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.