NA 0193-1900Recalls & reported problems
Stryker GmbH · Cutter Large · Class 1
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 07613252199953), received between Sep 9, 2015 and Sep 9, 2015 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2015Material Fragmentation
THE CUSTOMER REPORTED A BROKEN LARGE CUTTER T2 KIDS DURING SURGERY. THE ISSUE WAS NOTICED UNDER SURGERY OF A GIRL WITH ANTEBRACCIUM FRACTURE OF RADIUS AND ULNA, WHEN THE 2 NAIL WAS SUPPOSED TO BE CUT. THE CUSTOMER REPORTED THAT IT WAS A BIT TIGHT AND SUDDENLY IT BROKE INTO SEVERAL PIECES. THERE WERE NO DELAYS TO SURGERY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 5064811 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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