SCANLAN® Dennis Rib Cutter 9909-902Recalls & reported problems
Scanlan International Inc · SCANLAN® Dennis Rib Cutter 15mm Cut Height · Class 1
Data updated Oct 18, 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 00846159033694), received between Dec 13, 2024 and Dec 13, 2024 — classified as 1 malfunction.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 13, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE INSTRUMENT DID NOT CUT THE RIBS BUT CRUSHED THEM INSTEAD. THIS CAUSED AN ESTIMATED ADDITIONAL HOUR DURING THE SURGERY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY AND THE PATIENT DID HAVE A GOOD OUTCOME. THIS ISSUE OCCURED WITH THE FIRST USE OF THE INSTRUMENT. AS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20925676 ↗
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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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