AXSOS 661032SRecalls & reported problems
Stryker GmbH · Locking Screw · Class 2 · Implant
All models of AXSOS (184)
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 04546540685889), received between Nov 29, 2017 and Nov 29, 2017 — classified as 1 malfunction.
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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 29, 2017Break
DURING AXSOS TI SURGERY, THE DRILL BROKE. THE PATIENT BONE WAS SO HARD DUE TO THE CANCER. THE DRILL FRAGMENT WAS REMOVED FROM THE PATIENT. THE LOCKING SCREW BROKE WHEN THE SURGEON CHECKED THE SCREW LOCKING AND APPLIED TORQUE TO THE SCREW HEAD. THE SHAFT OF THE SCREW REMAINED IN THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 7068289 ↗
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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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