Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 19701–19720 of 27,655 recalls
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: Merge Hemo software. Product Usage: Merge Hemo is a hemodynamic Recalled by...
The Issue: In some instances, the system will lock tabs within a study, even when a...
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 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 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: 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: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: When taking measurements from images on the Cardio workstation or from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....
The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Care Systems Recalled by Merge Healthcare, Inc. Due to The system...
The Issue: The system will completely stop allowing the downloading or acquisition of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...
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: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...
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: 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: SpO2 connecting cable for Masimo LNCS sensor (Merge Part Number:...
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: 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. cannula...
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: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
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. Reamer....
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.