NA 2361-5075SRecalls & reported problems
Stryker GmbH · Advanced Locking Screw · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327381467), received between Oct 13, 2022 and Jul 6, 2026 — classified as 4 injuries.
The most frequently reported specific device problem is “Migration” (3 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Migration3
- Break1
- Device Dislodged or Dislocated1
- Fracture1
Patient problems
- Failure of Implant2
- Insufficient Information2
- Impaired Healing1
- Inadequate Osseointegration1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJul 6, 2026Migration
AS REPORTED: "AN ADVANCED LOCKING SCREW WAS IMPLANTED INTO A T2 ALPHA RETROGRADE NAIL FROM LATERAL TO MEDIAL DIRECTION ~(B)(6) 2026. FINAL II SHOTS SHOW THE SCREW WAS PLACED INTO THE NAIL AS PER OP TECH. (B)(6) 2026. PATIENT HAD TO BE REOPERATED TO REMOVE THE ADVANCE LOCKING SCREW AS IT HAS MIGRATED MEDIALLY WITH THE HEAD OF THE SCREW TOUCHING THE NAIL.".
Patient problems: Insufficient Information
MAUDE report 25724660 ↗InjurySep 15, 2023Break; Fracture; Break; Fracture
AS REPORTED: "T2 ALPHA FEMORAL RETROGRADE NAIL WAS FRACTURED AND DISTAL SCREWS WERE FRACTURED. ADVERSE CONSEQUENCES OF DELAYED FUSION AND REVISION SURGERY WERE REPORTED TOO."
Patient problems: Failure of Implant; Impaired Healing
MAUDE report 17760188 ↗InjuryMar 1, 2023Device Dislodged or Dislocated; Migration; Device Dislodged or Dislocated; Migration
IT WAS REPORTED THAT THE PATIENT WAS BROUGHT BACK TO REVISE AN INTERLOCKING SCREW THAT WAS BACKING OUT AND TAKE OUT ANTIBIOTIC SPACER. MINIFRAG AND SMALL FRAG PLATING, ALONG WITH BONE GRAFTING WERE USED DURING THE REVISION.
Patient problems: Inadequate Osseointegration; Insufficient Information
MAUDE report 16458559 ↗InjuryOct 13, 2022Migration; Migration
AS REPORTED: "POSTOPERATIVE BACK OUT OF THE SCREW".
Patient problems: Failure of Implant
MAUDE report 15594089 ↗
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- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
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- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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