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. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 501–520 of 47,938 recalls
Recalled Item: Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) SMJ LAP Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) CATH LAB Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) PACER / Recalled...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conductivity Standard Solution Catalog/Model Numbers: 10001 Recalled by...
The Issue: due to a defect associated with the conductivity values of the solution used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...
The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution. Recalled by...
The Issue: Fungal contamination of affected lot with Parengyodontium album.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes...
The Issue: Six (6) identified software issues which may result in the following: system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the Recalled...
The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. Recalled by Philips...
The Issue: It was found that the MX40 device could not reconnect to the PIC iX when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Recalled...
The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.