NA 55-06161Recalls & reported problems
Stryker Leibinger GmbH & Co. KG · ANCHOR PLATE,STANDARD,STRAIGHT,LONG · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540435675), received between May 11, 2021 and Apr 26, 2023 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Fracture” (2 reports).
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
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 26, 2023Fracture; Fracture
IT WAS REPORTED THE PLATE WAS IMPLANTED SUCCESSFULLY AND THEN LATER NOTICED THE PLATE HAD BROKE. A SECOND SURGERY WAS PERFORMED AND A TEMPORARY DEVICE WAS PUT IN PLACE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16815954 ↗MalfunctionMay 11, 2021Fracture; Fracture
IT WAS REPORTED BY THE COMPANY REPRESENTATIVE THAT IT WAS DISCOVERED DURING A SECOND SURGERY, THE PLATE WAS BROKEN. PLATE WAS REMOVED AND REPLACED. NO OTHER INFORMATION IS KNOWN AT THIS TIME.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11807811 ↗
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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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