XMCP 113-40032Recalls & reported problems
Extremity Medical, LLC · Lag Screw (solid) - 4.0 x 32 mm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842078102602), received between Jul 11, 2024 and Jul 11, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 11, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT THE SURGEON IMPLANTED THE PROXIMAL IMPLANT POST AND EVERYTHING WAS GOOD. HE MOVED TO THE DISTAL SIDE AND PREPARED THE JOINT AND BONE AS PER THE SURGICAL TECHNIQUE. HE THEN IMPLANTED THE DISTAL SCREW AND IT WAS TOO SMALL IN DIAMETER TO MAKE CORTICAL PURCHASE. THE SURGEON PROCEEDED TO PLACE HEADLESS COMPRESSION SCREWS ON EITHER SIDE OF THE IMPLANT.
Patient problems: Failure of Implant
MAUDE report 19725522 ↗
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- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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