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 11641–11660 of 27,512 recalls
Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremities Recalled by Medtronic Sofamor Danek USA Inc Due to Product may...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Child Starter Kits Recalled by Physio-Control, Inc. Due to Packaging...
The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant/Child Reduced Energy Defibrillation Electrodes Recalled by...
The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained...
The Issue: Abbott identified that samples tested for ARCHITECT STAT High Sensitive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Sterile Custom Kits packaged as a Piggy Back with Recalled by...
The Issue: DeRoyal manufactured procedure packs using BDPosiFlush syringes which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ShockPulse-SE Lithotripsy System Recalled by Olympus Corporation of...
The Issue: A component of the Olympus ShockPulse Transducer was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America, LLC Due to The thermo...
The Issue: The thermo switches in the three-phase transformer, which normally aid in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.