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 7521–7540 of 27,512 recalls
Recalled Item: Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Therapy Mask 3100 NC/SP Recalled by Philips Respironics, Inc. Due to No...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics DreamWear Full Face Mask Recalled by Philips...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clip COVID Rapid Antigen Test Kit (25-pack) Recalled by LUMINOSTICS, INC dba...
The Issue: COVID test kit shelf life was periodically extended, as real-time stability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starling Monitor Recalled by Baxter Healthcare Corporation Due to Labeling...
The Issue: Labeling has incorrect or incomplete Unique Device Identification (UDI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recreo Hair Growth Laser Comb Recalled by OMM Imports, Inc. dba Zero Gravity...
The Issue: The firm distributed the laser products without affixing the warning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Surgical Level 3 Gown Recalled by Texas Medical Technology Inc....
The Issue: Surgical gowns recalled due to gown fabric failing to pass the hydrostatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X ROVER MOBILE X-RAY SYSTEM Recalled by Micro-X Ltd. Due to Software...
The Issue: Software calibration error with product equip with a Dose Area Product (DAP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001...
The Issue: Drill Pin (drill bit) is not compatible with the Drill Template included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filter + Catheter Mount Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S with Expandi-Flex/Elbow: a) Recalled by TELEFLEX LLC Due...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR Power Knee OSSUR Power Knee Recalled by Ossur Americas Due to Battery...
The Issue: Battery may dislodge from the Power Knee
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....
The Issue: During internal testing, Leica Microsystems has become aware of a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.