Skip to content

NA 8919333Recalls & reported problems

Richard Wolf GmbH · TROCAR SLEEVE STRAI. CAP 5.5MM WL 62MM flexible plastic sheath with thread, distal tip straight, with membrane valve, with insufflation valve, reusable · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04055207021996), received between Oct 9, 2017 and Oct 9, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

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.

  • InjuryOct 9, 2017Device Contamination with Chemical or Other Material

    FOLLOW UP #2.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6932439 ↗

Other Trocar, gastro-urology devices

All Trocar, gastro-urology devices →

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