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NA 899750333Recalls & reported problems

Richard Wolf GmbH · RESECTOR AGGRESS Ø 3.7MM color code red, PACK = 1 PC, WL 130 mm, for use with motor handpieces M5/0 and M5/3, for soft tissue extraction, in Arthroscopy, reusable · Class 1

Data updated Oct 13, 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 04055207038376), received between May 5, 2017 and May 5, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • Foreign Body In Patient1
  • 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.

  • MalfunctionMay 5, 2017Break; Break

    FOLLOW UP #1.

    Patient problems: Foreign Body In Patient; No Known Impact Or Consequence To Patient

    MAUDE report 6547635 ↗

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Sources and updates

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