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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 8141–8160 of 27,512 recalls
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...
The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...
The Issue: The QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restrata Recalled by Acera Surgical Inc Due to Misprinted expiration date on...
The Issue: Misprinted expiration date on the shelf-box
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...
The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...
The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian...
The Issue: Software issue for treatment plan and image management application may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Gastrovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: regard Clinical Packaging...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.