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FASSIER-DUVAL TELESCOPIC IM SYSTEM FRT100Recalls & reported problems

Orthopediatrics Canada ULC · FEMALE RETRIEVER Ø3.2mm · Class 1

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 07540194007193), received between Jul 6, 2020 and Jul 6, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Device” (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.

Most reported problems

Device problems

  • Defective Device1
  • Difficult to Insert1
  • Failure to Align1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionJul 6, 2020Difficult to Insert; Failure to Align; Defective Device; Difficult to Insert; Failure to Align; Defective Device

    SURGEON INFORMED THAT DURING SURGERY IN A PATIENT WITH CONGENITAL PSEUDARTHROSIS, FOR REPLACING AN EXISTING FASSIER DUVAL NAIL BY A LARGER ONE, THE FEMALE RETRIEVER (FRT100) USED FOR THE REMOVAL PRESENTED A MISALIGNMENT OF THE TWO HALVES, CAUSING THAT THE INSTRUMENT DID NOT FIT WITH THE HEX HOLE OF THE IMPLANT TO BE REMOVED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10236693 ↗

Other EXTRACTOR devices

All EXTRACTOR devices →

Sources and updates

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