AVIATOR 48811116Recalls & reported problems
Stryker Corporation · ONE-LEVEL ANTERIOR PLATE · Class 2 · Implant
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 07613252152125), received between May 30, 2017 and May 30, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Bent” (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
- Bent1
- Break1
- Material Deformation1
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.
MalfunctionMay 30, 2017Bent; Break; Material Deformation; Material Deformation
IT WAS REPORTED THAT; ONE OF THE BARS FROM THE LOCKING MECHANISM OF THE AVIATOR PLATE WAS BENT AND SORT OF BROKEN. THE SURGEON NOTICED THE PLATE WAS AFTER IMPLANTING THE SCREWS AND WHEN HE LOOKED UNDER THE MICROSCOPE HE NOTICED THE BENT, ALMOST BROKEN BARS. SURGEON REMOVED THE SCREWS AND THE PLATE AND PUT ANOTHER PLATE IN. NO ADVERSE CONSEQUENCES TO THE PATIENT AND NO SURGICAL DELAY. PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6599812 ↗
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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 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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