Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,498 recalls have been distributed to Montana in the last 12 months.
Showing 11661–11680 of 27,852 recalls
Recalled Item: Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W Recalled by...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Premium Urine Meter Tray 400mL Recalled by Covidien Llc...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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.