NA 9734592Recalls & reported problems
Medtronic Powered Surgical Solutions · HAMMER 9734592 SLAP · Class 1
Data updated Oct 13, 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 00763000054281), received between Mar 11, 2020 and Mar 11, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Material Integrity Problem1
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.
MalfunctionMar 11, 2020Material Integrity Problem; Material Integrity Problem
MEDTRONIC RECEIVED INFORMATION REGARDING A NAVIGATION SYSTEM BEING USED DURING AN OBLIQUE LATERAL INTERBODY FUSION. IT WAS REPORTED THAT THE SLAP HAMMER WAS BROKEN DUE TO EXCESSIVE POWER, WHILE BEING USED INSIDE THE PATIENT. IT WAS NOTED THAT THE TRIAL WAS REMOVED USING OTHER INSTRUMENTS. THERE WAS NO SURGICAL DELAY AND NO IMPACT ON PATIENT OUTCOME.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9818140 ↗
Other HAMMER, SURGICAL devices
- NA A6779Depuy (Ireland) · HAMMER, SURGICAL128 reports
- SUMMIT 2570-05-250Depuy (Ireland) · HAMMER, SURGICAL100 reports
- NA 03.010.522Synthes GmbH · HAMMER, SURGICAL68 reports
- NA 399.42Synthes GmbH · HAMMER, SURGICAL39 reports
- NA 399.43Synthes GmbH · HAMMER, SURGICAL37 reports
- NA 03.010.170Synthes GmbH · HAMMER, SURGICAL37 reports
- NA 359.218Synthes GmbH · HAMMER, SURGICAL35 reports
- NA 03.010.056Synthes GmbH · HAMMER, SURGICAL27 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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