ANCHORAGE PLSL3012Recalls & reported problems
Stryker GmbH · Locking Screw · Class 2 · Implant
All models of ANCHORAGE (52)
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 07613252262114), received between Feb 7, 2020 and Jul 6, 2021 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Difficult to Insert” (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
- Difficult to Insert1
- Migration1
Patient problems
- Failure of Implant1
- Implant Pain1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 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 12122250 ↗MalfunctionFeb 7, 2020Difficult to Insert; Difficult to Insert
IT WAS REPORTED THAT A 3.0MM LOCKING SCREW WENT STRAIGHT THROUGH THE HOLE OF AN ANCHORAGE MTP FUSION PLATE. WHILE INSERTING THE SCREW IN THE PLATE TO ACHIEVE FIXATION THE 3.0 LOCKING SCREW DID NOT LOCK INTO PLACE AND PROCEEDED TO GO BEYOND THE PLATE INTO THE BONE. A NEW SCREW WAS USED WITH SUCCESS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9684859 ↗
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- 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-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive 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-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive 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 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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