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ANCHORAGE PLSS3522Recalls & reported problems

Stryker GmbH · Non Locking Screw · Class 2 · Implant

All models of ANCHORAGE (52)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613252262961), received between Aug 29, 2018 and Jun 6, 2019 — classified as 3 injuries, 1 malfunction.

The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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

  • Adverse Event Without Identified Device or Use Problem3
  • Activation, Positioning or Separation Problem1

Patient problems

  • Tissue Damage3
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem

    SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY (B) (6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.

    Patient problems: Tissue Damage

    MAUDE report 8675269 ↗
  • InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem

    SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY (B)(6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.

    Patient problems: Tissue Damage

    MAUDE report 8675266 ↗
  • InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem

    SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY (B)(6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.

    Patient problems: Tissue Damage

    MAUDE report 8675186 ↗
  • MalfunctionAug 29, 2018Activation, Positioning or Separation Problem

    IT WAS REPORTED THAT SURGEON WAS PERFORMING AN ORIF MID FOOT ARTHRODESIS PROCEDURE - RIGHT SIDE AND WAS ATTEMPTING TO IMPLANT A 3.5 ANCHORAGE SCREW, AND THE SCREW WENT THROUGH THE HOLE IN THE PLATE AND PROCEEDED TO GO ALL THE WAY THROUGH THE PLATE OUT THE BACK SIDE. SURGEON REMOVED PLATE AND SCREW AND WENT BACK IN WITH A NEW PLATE AND SCREWS AND COMPLETED THE CASE SUCCESSFULLY AND WITH NO DELAY OR ADVERSE CONSEQUENCE TO THE PATIENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7827325 ↗

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

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