ANCHORAGE PLSL3514Recalls & reported problems
Stryker GmbH · Locking Screw · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613252262343), received between Feb 24, 2020 and Dec 4, 2025 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Difficult to Insert” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Difficult to Insert4
- Positioning Failure2
- Fracture1
- Material Deformation1
- Naturally Worn1
Patient problems
- No Consequences Or Impact To Patient4
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 4, 2025Fracture; Material Deformation; Fracture; Material Deformation
IT WAS REPORTED THAT "WHEN REMOVING THE LISFRANC PLATE, THE HEADS OF THE SCREWS BREAK 3.5 MM."
Patient problems: Insufficient Information
MAUDE report 23720331 ↗MalfunctionAug 31, 2021Positioning Failure; Positioning Failure
IT WAS REPORTED THAT THE TWO LOCKING SCREWS DID NOT LOCK INTO THE PLATE HOLES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12391377 ↗MalfunctionJul 30, 2020Positioning Failure; Naturally Worn; Positioning Failure; Naturally Worn
IT WAS REPORTED, LOCKING THREADS WERE WORN DOWN AND DIDN'T LOCK INTO PLATE, NEXT SCREW WORKED PERFECTLY. DOCTOR WASN'T LIKING HOW IT SAT ON PLATE, PULLED IT OUT AND PUT IN A NEW ONE AND IT WORKED BETTER. AFTER EXAMINING THE SCREW HE DETERMINED IT WAS THE THREADS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10347966 ↗MalfunctionFeb 24, 2020Difficult to Insert; Difficult to Insert
PLATE FAILED TO ACCEPT LOCKING SCREWS. PROLONGED THE CASE BY 5 MINUTES TO SWITCH TO DIFFERENT PLATE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9748425 ↗MalfunctionFeb 24, 2020Difficult to Insert; Difficult to Insert
PLATE FAILED TO ACCEPT LOCKING SCREWS. PROLONGED THE CASE BY 5 MINUTES TO SWITCH TO DIFFERENT PLATE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9748409 ↗MalfunctionFeb 24, 2020Difficult to Insert; Difficult to Insert
PLATE FAILED TO ACCEPT LOCKING SCREWS. PROLONGED THE CASE BY 5 MINUTES TO SWITCH TO DIFFERENT PLATE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9748403 ↗MalfunctionFeb 24, 2020Difficult to Insert; Difficult to Insert
PLATE FAILED TO ACCEPT LOCKING SCREWS. PROLONGED THE CASE BY 5 MINUTES TO SWITCH TO DIFFERENT PLATE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9748402 ↗
Other PLATE, FIXATION, BONE devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-DRF32Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page