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PHALINX 45A01001Recalls & reported problems

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

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 00889797102131), received between Sep 11, 2023 and Sep 11, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Difficult to Remove1
  • Mechanical Jam1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 11, 2023Difficult to Remove; Mechanical Jam; Difficult to Remove; Mechanical Jam

    AS REPORTED: WE OPENED AN XS AND THE DOCTOR COULDN'T REMOVE THE IMPLANT FROM THE HANDLE. AFTER FURTHER EXAMINE/TRYING TO PULL OUT THE IMPLANT WITH DIFFERENT INSTRUMENTS, WE REALIZED THE IMPLANT WAS STUCK AND LOOKED LIKE 75% OF THE IMPLANT WAS PUSHED INTO THE HANDLE VS THE TYPICAL 50%. ENDED UP OPENING ANOTHER XS AND USED IT."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17726052 ↗

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.