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RUSCH IPN048378Recalls & reported problems

Teleflex Incorporated · RUSCH GREENLITE SU MTL BLADE MILL 0 · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14026710625992), received between Apr 22, 2022 and Apr 22, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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

  • Break2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 22, 2022Break; Break

    IT WAS REPORTED "BROKEN LIGHT PIPE IN BAG PRIOR TO USE AND BROKEN LIGHT PIPE AT TIME OF USE ON SECOND BLADE." CLARIFYING INFORMATION RECEIVED FROM CUSTOMER STATED THAT THERE WAS NO PATIENT INVOLVEMENT WHEN ISSUE WAS OBSERVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14189278 ↗
  • MalfunctionApr 22, 2022Break; Break

    IT WAS REPORTED "BROKEN LIGHT PIPE IN BAG PRIOR TO USE AND BROKEN LIGHT PIPE AT TIME OF USE ON SECOND BLADE." CLARIFYING INFORMATION RECEIVED FROM CUSTOMER STATED THAT THERE WAS NO PATIENT INVOLVEMENT WHEN ISSUE WAS OBSERVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14189219 ↗

Other LARYNGOSCOPE, RIGID devices

All LARYNGOSCOPE, RIGID devices →

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