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. 2,529 recalls have been distributed to North Dakota in the last 12 months.
Showing 10721–10740 of 47,938 recalls
Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...
The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Progressa Bed System Recalled by Baxter Healthcare Corporation Due...
The Issue: The compression links on impacted Progressa beds, listed in Appendix A, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate PhenoTest BC kit Recalled by Accelerate Diagnostics Inc Due to...
The Issue: Due improperly formulated and released bulk lot of fluorescence in situ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope...
The Issue: Broken Optical fiber cable damage can occur through handling or bending and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18239: ASM Omnipod Dash PDM Recalled by Insulet Corporation Due to The firm...
The Issue: The firm has become aware of PDM battery issues, including battery swelling,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to...
The Issue: Two electronic diode components (D1 & D4) placed in the reverse orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Tabletop for Operating Table System 1140 Recalled by Getinge Usa...
The Issue: The back rest may unintentionally drop suddenly, resulting in adverse health...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER...
The Issue: Due to a defect in the outer pouch sterile seal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System APM Procedure Instrument with Matrix Recalled by Sonendo...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tobramycin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ofloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GONAK Hypromellose Ophthalmic Demulcent Solution Recalled by Akorn, Inc. Due...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Ophthalmic Solution 0.5% Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Akorn, Inc. Due to...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tobramycin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.