NA 2598-07-580Recalls & reported problems
Depuy Orthopaedics, Inc. · TISSUE SPARING SOLUTIONS THREADED SLAP HAMMER ADAPTER · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295148555), received between Feb 28, 2020 and Apr 24, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Most reported problems
Device problems
- Break1
- Entrapment of Device1
- Naturally Worn1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2020Naturally Worn; Naturally Worn
THE INSTRUMENT WAS IDENTIFIED BY THE HOSPITAL AS WEAR AND TEAR OF THE TIP OF THE CORAIL THREADED ADAPTER AND THE HOSPITAL HAS DISPOSED OF THE INSTRUMENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9996084 ↗MalfunctionFeb 28, 2020Break; Entrapment of Device; Break; Entrapment of Device
IT WAS REPORTED THAT THE TIP OF THE SLAP HAMMER BROKE .BROKE OFF WHILE REMOVING A SUMMIT HIP STEM. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9772008 ↗
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 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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