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. 2,503 recalls have been distributed to North Dakota in the last 12 months.
Showing 12541–12560 of 47,938 recalls
Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...
The Issue: The nickel-sensitivity statement on the outer carton may be partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code:...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Uretero-reno videoscope Recalled by Olympus Corporation of the...
The Issue: The bending section of the URF-V2 may crack, resulting in an abnormal shape...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and...
The Issue: Products do not meet length and diameter specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Medtronic formerly...
The Issue: The audible alarm may not sound and/or the omni-directional LED visual alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution 1.5% w/w Recalled by Preferred...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit Recalled by Wilton...
The Issue: Milk is missing from the product's allergen Contains statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...
The Issue: QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GONADORELIN (5ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc., dba APS...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable Recalled by Drug...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Dissolution Specifications; during long term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable Recalled by Drug...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.