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. 2,404 recalls have been distributed to North Dakota in the last 12 months.
Showing 18981–19000 of 27,512 recalls
Recalled Item: Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fruit Punch Glucose Recalled by Azer Scientific, Inc. Due to Out of...
The Issue: Out of Specification Microbiological test results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucose Tolerance Beverage- Orange 50 gram Concentration Recalled by Azer...
The Issue: Out of Specification Microbiological test results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...
The Issue: Siemens received multiple customer complaints indicating an increase in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences has been notified of a medical device recall by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM) Recalled by Siemens...
The Issue: Siemens received multiple customer complaints indicating an increase in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...
The Issue: The infant performance test did not meet the test specification for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...
The Issue: Misbranded: Incorrect etching on the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...
The Issue: Casters on the EKOS carts may be missing washers which can cause premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...
The Issue: Incorrect label on the Sertera Biopsy Kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 Recalled by Panoramic Rental Corp. Due to...
The Issue: Panoramic Corporation is performing a voluntary Medical Device Correction on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Used to make treatment plans for patients Recalled by...
The Issue: In a specific workflow where contours are edited (enlarged, moved, copied,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.