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PHALINX 45A01004Recalls & reported problems

Wright Medical Technology, Inc. · Cannulated Straight · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889797102162), received between Dec 4, 2023 and Dec 4, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Mechanical Jam” (2 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 2 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Mechanical Jam2
  • Positioning Failure2
  • Separation Failure2
  • Unstable2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 4, 2023Positioning Failure; Unstable; Separation Failure; Mechanical Jam; Positioning Failure; Unstable; Separation Failure; Mechanical Jam

    THE PATIENT HAD HAMMERTOES ON 2ND & 3RD DIGITS THAT NEEDED FIXATION. IT WAS REPORTED THAT THE IMPLANTS DID NOT WANT TO COME OFF OF THE HANDLES AND THE DRILL BITS DID NOT WANT TO DETACH FROM THE HANDLES EITHER TO DRILL USING POWER. IT TOOK APPROXIMATELY 10-15 MINUTES LONGER DUE TO HAVING TO PRY THE IMPLANT AND DRILL FROM THEIR HANDLES. AND THE IMPLANT WAS PUT IN TO THE MIDDLE PHALANX THREE TIMES ON THE 2ND DIGIT AND IT PULLED OUT WITH THE HANDLE EACH TIME. IT WAS LOOSE AND SECURED WITH K WIRE. THE 3RD DIGIT WAS IMPLANTED WITHOUT THE USE OF THE HANDLE IN THE KIT AND WENT SMOOTHLY MINUS ISSUES REMOVING THE IMPLANT FROM THE HANDLE. BONE QUALITY IN PATIENT APPEARED TO BE GOOD AS HE HAD TO USE SOME EFFORT WHEN DRILLING USING POWER. WHEN THE IMPLANT WAS SCREWED INTO THE MIDDLE PHALANX AND FULLY SEATED HE FELT THAT THERE WAS A GOOD AMOUNT OF BITE, BUT WHEN THE HANDLE WAS PULLED BACK IT WOULD NOT RELEASE THE IMPLANT. THIS CAUSED THE IMPLANT TO PULL OUT OF THE MIDDLE PHALANX AND IT REMOVED BONE WITH IT. THIS WAS ATTEMPTED THREE TIMES BEFORE PULLING THE IMPLANT OUT OF THE HANDLE WHICH REQUIRED SOME FORCE AND THEN IT WAS INSERTED USING FORCEPS. DEVICE DID NOT APPEAR TO BE BROKEN AND NO OTHER C

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18263585 ↗
  • InjuryDec 4, 2023Positioning Failure; Unstable; Separation Failure; Mechanical Jam; Positioning Failure; Unstable; Separation Failure; Mechanical Jam

    THE PATIENT HAD HAMMERTOES ON 2ND AND 3RD DIGITS THAT NEEDED FIXATION. IT WAS REPORTED THAT THE IMPLANTS DID NOT WANT TO COME OFF OF THE HANDLES AND THE DRILL BITS DID NOT WANT TO DETACH FROM THE HANDLES EITHER TO DRILL USING POWER. IT TOOK APPROXIMATELY 10-15 MINUTES LONGER DUE TO HAVING TO PRY THE IMPLANT AND DRILL FROM THEIR HANDLES. AND THE IMPLANT WAS PUT IN TO THE MIDDLE PHALANX THREE TIMES ON THE 2ND DIGIT AND IT PULLED OUT WITH THE HANDLE EACH TIME. IT WAS LOOSE AND SECURED WITH K WIRE. THE 3RD DIGIT WAS IMPLANTED WITHOUT THE USE OF THE HANDLE IN THE KIT AND WENT SMOOTHLY MINUS ISSUES REMOVING THE IMPLANT FROM THE HANDLE. BONE QUALITY IN PATIENT APPEARED TO BE GOOD AS HE HAD TO USE SOME EFFORT WHEN DRILLING USING POWER. WHEN THE IMPLANT WAS SCREWED INTO THE MIDDLE PHALANX AND FULLY SEATED HE FELT THAT THERE WAS A GOOD AMOUNT OF BITE, BUT WHEN THE HANDLE WAS PULLED BACK IT WOULD NOT RELEASE THE IMPLANT. THIS CAUSED THE IMPLANT TO PULL OUT OF THE MIDDLE PHALANX AND IT REMOVED BONE WITH IT. THIS WAS ATTEMPTED THREE TIMES BEFORE PULLING THE IMPLANT OUT OF THE HANDLE WHICH REQUIRED SOME FORCE AND THEN IT WAS INSERTED USING FORCEPS. DEVICE DID NOT APPEAR TO BE BROKEN AND NO OTHER

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18263498 ↗

Other PIN, FIXATION, SMOOTH devices

All PIN, FIXATION, SMOOTH devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.