CHARNLEY 9620-72-000Recalls & reported problems
Depuy International Ltd · CHARNLEY SAW EX FLEXIBLE 50CM · Class 1
All models of CHARNLEY (5)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295241058), received between Mar 7, 2019 and Mar 14, 2019 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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
Device problems
- Break3
Patient problems
- Not Applicable3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 14, 2019Break; Break
MalfunctionMar 7, 2019Break; Break
WE HAD A PROBLEM WITH 3 DIFFERENT GIGLI SAWS ON FRIDAY AFTERNOON.
Patient problems: Not Applicable
MAUDE report 8398818 ↗MalfunctionMar 7, 2019Break; Break
WE HAD A PROBLEM WITH 3 DIFFERENT GIGLI SAWS ON FRIDAY AFTERNOON.
Patient problems: Not Applicable
MAUDE report 8398778 ↗
Other SAW devices
- NA 511.912SSynthes GmbH · SAW1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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