RUSCH IPN915486Recalls & reported problems
Teleflex Incorporated · RUSCH STANDARD HANDLE: MEDIUM · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 14026704711663), received between Feb 21, 2023 and Feb 21, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Environmental Compatibility Problem” (3 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
- Environmental Compatibility Problem3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 21, 2023Environmental Compatibility Problem; Environmental Compatibility Problem
CUSTOMER CALLED STATING THAT THE LIGHT WOULD NOT WORK WHEN THE BLADE IS ATTACHED. THEY HAVE CHANGED THE BLUBS AND BATTERIES, NO CHANGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16409582 ↗MalfunctionFeb 21, 2023Environmental Compatibility Problem; Environmental Compatibility Problem
CUSTOMER CALLED STATING THAT THE LIGHT WOULD NOT WORK WHEN THE BLADE IS ATTACHED. THEY HAVE CHANGED THE BLUBS AND BATTERIES, NO CHANGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16409570 ↗MalfunctionFeb 21, 2023Environmental Compatibility Problem; Environmental Compatibility Problem
CUSTOMER CALLED STATING THAT THE LIGHT WOULD NOT WORK WHEN THE BLADE IS ATTACHED. THEY HAVE CHANGED THE BLUBS AND BATTERIES, NO CHANGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16409567 ↗
Other LARYNGOSCOPE, RIGID devices
- McGRATH MAC 301-000-000Covidien LP · LARYNGOSCOPE, RIGID2 recalls202 reports
- McGRATH MAC 300-000-000Covidien LP · LARYNGOSCOPE, RIGID1 recall1 death205 reports
- n.a. 8404HXKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID242 reports
- McGRATH 340-000-000Covidien LP · LARYNGOSCOPE, RIGID2 deaths192 reports
- McGRATH MAC 301-000-000Covidien LP · LARYNGOSCOPE, RIGID2 recalls90 reports
- n.a. 8404BXCKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID141 reports
- n/a 8404AXCKarl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID108 reports
- McGRATH 340-000-000Covidien LP · LARYNGOSCOPE, RIGID84 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.