AVIATOR 48811224Recalls & reported problems
Stryker Corporation · TWO-LEVEL ANTERIOR PLATE · Class 2 · Implant
Data updated Oct 13, 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 07613252152163), received between Nov 30, 2017 and Jan 26, 2018 — classified as 2 malfunctions.
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
- Device Operates Differently Than Expected1
- Failure to Advance1
- Mechanical Problem1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 26, 2018Bent; Failure to Advance
IT WAS REPORTED THAT THE DOCTOR ATTEMPTED TO USE A 2 LEVEL PLATE ON FRIDAY AND AS HE WAS ADVANCING THE FIRST SCREW, THE LOCKING WING WOULD NOT ALLOW IT TO PASS AND BENT DOWNWARD WITH THE SCREW. HE WAS NOT OVER ANGULATING THE SCREW AND WE MADE SURE THE WINGS WERE IN THE UNLOCK POSITION. IT WAS A C5-7 ACDF.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7223077 ↗MalfunctionNov 30, 2017Mechanical Problem; Device Operates Differently Than Expected; Mechanical Problem
IT WAS REPORTED THAT THE LOCKING MECHANISM WOULD NOT LOCK ON ONE SIDE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7070752 ↗
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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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