CHARNLEY 9620-45-000Recalls & reported problems
Depuy International Ltd · CHARNLEY CURETTE SML · Class 1
All models of CHARNLEY (5)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295240853), received between Feb 20, 2019 and Feb 20, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
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 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Loose or Intermittent Connection1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 20, 2019Loose or Intermittent Connection; Detachment of Device or Device Component; Loose or Intermittent Connection; Detachment of Device or Device Component
T-BAR HAS DIS-ASSEMBLED FROM THE INSTRUMENT (T-BAR NOT BROKEN).
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8353760 ↗
Other CURETTE devices
- Centurion I68480Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68380Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67600KCenturion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I67970Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68040Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 66745Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67050Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67430Centurion Medical Products Corporation · CURETTE1 recall0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page