CANON INC. CXDI-401C COMPACTRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04549292049695), received between Dec 22, 2019 and Dec 22, 2019 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Misassembly During Maintenance/Repair” (3 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 22, 2019Misassembly During Maintenance/Repair; Misassembly During Maintenance/Repair

  AFTER UPDATING THE CONTROL SOFTWARE FOR X-RAY DETECTORS (CXDI-401C COMPACT/701C WIRELESS), THE CAPTURED IMAGE COULD NOT BE SEND TO PACS SYSTEM, AND THEN EVENTUALLY THE IMAGE DISAPPEARED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9508741 ↗
• MalfunctionDec 22, 2019Misassembly During Maintenance/Repair; Misassembly During Maintenance/Repair

  AFTER UPDATING THE CONTROL SOFTWARE FOR X-RAY DETECTORS (CXDI-401C COMPACT/701C WIRELESS), THE CAPTURED IMAGE COULD NOT BE SEND TO PACS SYSTEM, AND THEN EVENTUALLY THE IMAGE DISAPPEARED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9508740 ↗
• MalfunctionDec 22, 2019Misassembly During Maintenance/Repair; Misassembly During Maintenance/Repair

  AFTER UPDATING THE CONTROL SOFTWARE FOR X-RAY DETECTORS (CXDI-401C COMPACT/701C WIRELESS), THE CAPTURED IMAGE COULD NOT BE SEND TO PACS SYSTEM, AND THEN EVENTUALLY THE IMAGE DISAPPEARED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9508737 ↗