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. 2,415 recalls have been distributed to North Dakota in the last 12 months.
Showing 18301–18320 of 27,512 recalls
Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) Recalled by...
The Issue: The affected products have approximately a 91% specificity while the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number...
The Issue: Maquet has received 3 confirmed complaints related to the Li-lon Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...
The Issue: Cross profile for Varian 60 degree wedge shows "horns."
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...
The Issue: Power outages causes reporting software to shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...
The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...
The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K2 Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias results with the IMMULITE¿ /IMMULITE¿ 1000 Third Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.