ANCHORAGE PLSS3030Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613252262824), received between Jul 23, 2018 and Jul 6, 2021 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Migration” (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
- Migration2
- Break1
Patient problems
- Failure of Implant2
- Implant Pain2
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJul 6, 2021Migration; Migration
IT WAS REPORTED THROUGH THE FILING OF A LAWSUIT THAT ALLEGEDLY ON OR ABOUT (B)(6) 2019 THE PATIENT UNDERWENT FOOT SURGERY. IT IS FURTHER ALLEGED THAT THE PATIENT DEVELOPED PAIN AND ON OR ABOUT (B)(6) 2019 IT WAS DISCOVERED THAT THE SCREWS HAD COME LOOSE. IT IS ALLEGED THAT REVISION SURGERY WAS REQUIRED TO RE-DO THE PROCEDURE.
Patient problems: Failure of Implant; Implant Pain
MAUDE report 12122243 ↗InjuryJul 6, 2021Migration; Migration
IT WAS REPORTED THROUGH THE FILING OF A LAWSUIT THAT ALLEGEDLY ON OR ABOUT (B(6) 2019 THE PATIENT UNDERWENT FOOT SURGERY. IT IS FURTHER ALLEGED THAT THE PATIENT DEVELOPED PAIN AND ON OR ABOUT (B)(6) 2019 IT WAS DISCOVERED THAT THE SCREWS HAD COME LOOSE. IT IS ALLEGED THAT REVISION SURGERY WAS REQUIRED TO RE-DO THE PROCEDURE.
Patient problems: Failure of Implant; Implant Pain
MAUDE report 12122241 ↗MalfunctionJul 23, 2018Break
HEAD BROKE OFF OF A 3.0 NON LOCKING SCREW THROUGH AN ANCHORAGE PLATE DURING A CASE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7712222 ↗
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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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