Jones Screw 142-45035Recalls & reported problems
Extremity Medical, LLC · 5th Metatarsal Screw, 4.5 x 35 mm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842078115329), received between Nov 21, 2024 and Nov 21, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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
- Inadequacy of Device Shape and/or Size1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 21, 2024Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
IT WAS REPORTED THAT THE SURGEON BROKE THE MEDIAL CORTICAL WALL WHEN ADVANCING THE SCREW FOR A SMALL FEMALE PATIENT AND HAD TO BAIL OUT WITH A LONGER 4.0 HEADLESS SCREW. THE SURGEON USED THE REAMERS, BUT NOT DID NOT USE THE TAP. THE AP AND LATERAL VIEWS LOOKED OK FOR THE GUIDE WIRE AND REAMER. IT LOOKED LIKE THE CORRECT DIAMETER FOR THE PATIENT (4.5MM), BUT HIS FIRST K-WIRE WAS OUT OF THE MEDULLARY CANAL MEDIALLY AND THE SCREW JUST FOLLOWED THE SAME PATH. THE SURGEON SAID HE WAS "FIGHTING THE PATIENT'S FOOT PROXIMALLY". THE REP INDICATED THAT THE SURGEON DIDN'T HAVE THE "REAL ESTATE" TO BRING HIS HANDS MORE MEDIALLY.
Patient problems: Bone Fracture(s)
MAUDE report 20750646 ↗
Other Screw, Fixation, Bone devices
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- 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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