Skip to content

SPECIALIST 96-6136Recalls & reported problems

Depuy (Ireland) · SPECIALIST 2 ANTERIOR DOWN SIZING GUIDE SZ 1.5-6 · Class 1

All models of SPECIALIST (80)

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 10603295246961), received between Sep 29, 2022 and Sep 29, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Jam” (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

  • Mechanical Jam1
  • Naturally Worn1

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 29, 2022Mechanical Jam; Naturally Worn; Mechanical Jam; Naturally Worn

    IT WAS REPORTED THAT THE BUTTON ON THE SIDE OF THE SIZING GUIDE IS JAMMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15508355 ↗

Other TEMPLATE devices

All TEMPLATE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page