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. 2,553 recalls have been distributed to North Dakota in the last 12 months.
Showing 4481–4500 of 27,512 recalls
Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chiba Biopsy Needle - Used for aspiration biopsy. PART Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete Recalled...
The Issue: The reason for the recall is the pneumatic tubing used in the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...
The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...
The Issue: Products were found to have confirmed drug cross contamination prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Structural Balloon Trocar Recalled by Covidien, LP Due...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.