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. 972 recalls have been distributed to North Dakota in the last 12 months.
Showing 25701–25720 of 47,938 recalls
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.54% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.82% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Functionality in the report sections "Findings Information" and "Summary of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use...
The Issue: Urea Nitrogen reagent kit demonstrated an increased incidence of Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Care Calcium Chews Recalled by Bestco, Inc. Due to A packaging...
The Issue: A packaging revision and lack of revision to the corresponding packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...
The Issue: These one-way valves may disconnect at the joint between the two components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDim Eleva 708032 As a multifunctional universal imaging application...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smooth Guide Wire Bullet Tip 3.0 mm Diameter Recalled by Zimmer Biomet, Inc....
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.