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. 1,900 recalls have been distributed to Montana in the last 12 months.
Showing 13781–13800 of 48,326 recalls
Recalled Item: Rizatriptan Benzoate Film Coated Tablets Recalled by MACLEODS PHARMA USA,...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 10mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 5mg Recalled by MACLEODS...
The Issue: Out-of-specification test results obtained in Organic Impurities test during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600 Recalled by...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roberts Digital VIPR System (with E-size cylinder) Model: ROC-9840 Recalled...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Western Oxytote DTE Digital VIPR System (with D-size cylinder) Model:...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Western Oxytote DTE Digital VIPR System (with E-size cylinder) Model:...
The Issue: VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Udel Sterilization Tray Instructions for Use Recalled by Karl...
The Issue: To ensure sterilization effectiveness, sterilization tray instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: These are communication systems Recalled by Hill-Rom Inc. Due to An...
The Issue: An unrecoverable error may occur where a component will fail to complete the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 Recalled by...
The Issue: When the ultrasound system is used in combination with a Fujifilm (formally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPL Coupling Gel Recalled by Lumenis, Inc. Due to Ultrasound gels and...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.