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. 2,356 recalls have been distributed to Montana in the last 12 months.
Showing 33241–33260 of 48,326 recalls
Recalled Item: Merge Eye Station Import Utility (ESIU). The firm name on Recalled by Merge...
The Issue: System locks up which may result in potential patient injury or delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...
The Issue: The versions allow images to be stored without pixel data, resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Recalled by Merge Healthcare, Inc. Due to Cardio...
The Issue: Cardio study list does not show STAT studies without .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...
The Issue: The software produced a number of "do not route" exceptions, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station and Merge Eye Care PACS. Recalled by Merge Healthcare,...
The Issue: During an antivirus program scan of the Eye Station or Eye Care PACS, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. The firm name on the labeling is Merge Healthcare...
The Issue: Use of the software may show an incorrect value to the user when viewing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...
The Issue: Under certain conditions, the cables used with the Hemo system during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...
The Issue: An error message can occur resulting in the prior studies being unavailable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Chorionic Gonadotropin Recalled by Complete Pharmacy and Medical...
The Issue: Non-sterility - presence of bacteria confirmed by outside laboratory after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. guide Recalled...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Rod Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...
The Issue: Reports of failure of the device's power supply.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Appliance...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Arthroscope....
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity...
The Issue: Philips Healthcare received reports from the field that certain Ingenuity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Bit Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp...
The Issue: Increased customer complaints indicating inconsistent clip application; may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.