NA 2361-5030SRecalls & reported problems
Stryker GmbH · Advanced Locking Screw · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327381498), received between Nov 3, 2023 and Jul 20, 2026 — classified as 3 injuries.
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
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Limb Fracture2
- Bone Fracture(s)1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJul 20, 2026Adverse Event Without Identified Device or Use Problem
As reported: "Removal surgery was performed due to secondary fracture occurred in the femoral trochanteric region ipsilateral to the site of the implanted nail after bone union was achieved."
Patient problems: Limb Fracture
MAUDE report 25882082 ↗InjuryJul 20, 2026Adverse Event Without Identified Device or Use Problem
AS REPORTED: "REMOVAL SURGERY WAS PERFORMED DUE TO SECONDARY FRACTURE OCCURRED IN THE FEMORAL TROCHANTERIC REGION IPSILATERAL TO THE SITE OF THE IMPLANTED NAIL AFTER BONE UNION WAS ACHIEVED."
Patient problems: Limb Fracture
MAUDE report 25881799 ↗InjuryNov 3, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: "BONE FRACTURE OCCURRED ALONG THE ADVANCED LOCKING SCREW INSERTION POSITION. SCREW INSERTION WAS PERFORMED AFTER 4.2MM DRILL FOLLOWED COUNTERBORE DRILLING.".
Patient problems: Bone Fracture(s)
MAUDE report 18065669 ↗
Other Screw, fixation, bone devices
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- Control 360 SK12Treace Medical Concepts, Inc. · Screw, Fixation, Bone195 reports
- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- 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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