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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 8021–8040 of 47,938 recalls
Recalled Item: Olympus Airway Mobilescope Recalled by Olympus Corporation of the Americas...
The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-MR1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...
The Issue: Degrading capacitors on the control board of ventilators and spare parts may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...
The Issue: The outer package labeling and product etch are for a Size 6, however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sausage Maker Instacure #1 Recalled by The Sausage Maker, Inc. Due to...
The Issue: Contains Sodium Nitrite recalled for potential metal contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...
The Issue: During rework of components during the manufacturing process, an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...
The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...
The Issue: Ground cable installed incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...
The Issue: Sterility of device may be compromised due to breach of the chevron seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Recalled...
The Issue: CGMP deviation: product released prior to supplier approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...
The Issue: cGMP deviations: Batch was released prior to approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...
The Issue: cGMP deviations: Batch was released prior to approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...
The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...
The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenition 70. The device is to be used in health Recalled by Philips Medical...
The Issue: Philips has become aware of the potential for unintended radiation exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.