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AXSOS 627540Recalls & reported problems

Stryker GmbH · Locking Compression Plate Narrow · Class 2 · Implant

All models of AXSOS (184)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327174908), received between Jun 22, 2018 and Jun 22, 2018 — classified as 1 injury.

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
  • Fracture1

Patient problems

  • Fall1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 22, 2018Break; Fracture

    THIS PI IS FOR THE PLATE AND SCREWS REVISED ON (B)(6) 2018. THE SURGEON REVISED A HIP REPLACEMENT ORIGINALLY DONE (B)(6) 2018 VIA MAKO. THE PATIENT HAD A AXSOS PLATE AND DAL-MILE CABLES ADDED ON (B)(6) 2018 AND THEN HAD RECENTLY FALLEN AND BROKE THE PLATE AND FRACTURED THE FEMUR JUST BELOW THE STEM. THE SURGEON REMOVED THE PLATE/SCREWS/STEM AND HEAD AND KEPT THE ORIGINAL CUP AND LINER IN. HE CHANGED TO A CONE/CONICAL STEM WITH A NEW HEAD. UPDATE (B)(6) 2018: SPOKE TO REP. CABLES WERE ALSO EXPLANTED. REP PROVIDED USAGE FORMS AND X-RAYS, AND REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE DUE TO HOSPITAL POLICY.

    Patient problems: Fall

    MAUDE report 7628715 ↗

Other Plate, fixation, bone devices

All Plate, fixation, bone devices →

Sources and updates

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