Welch Allyn, Inc. 901038 (REF 69696)Recalls & reported problems

Welch Allyn, Inc. · Welch Allyn MacIntosh 2.5 V Halogen HPX Fiber-Optic Laryngoscope Set; Green Standard (ISO 7376), Stainless Steel, Blade Sizes #1 to #4 (Qty. 4), Medium C-Cell Power Handle, Small AA-Cell Power Handle, Hard Storage Case · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

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.

Recalls naming this device

May 17, 2022Class IITerminated
Packaging error.
Z-1288-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Device details

UDI-DI	`00732094141078`
Brand	Welch Allyn, Inc.
Model	901038
Catalog no.	69696
Company	Welch Allyn, Inc.
Product code	CCW · LARYNGOSCOPE, RIGID
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Aug 31, 2023

Device type (GMDN): Rigid intubation laryngoscope, reusable

A hand-held device intended to be used by anaesthesia/emergency service personnel to manipulate the tongue, preventing it from obstructing the oropharynx and enabling a clear view of the trachea for the insertion of an endotracheal (ET) tube prior to the delivery of inhalation anaesthesia and/or ventilation. It has a handle containing batteries to power its light (a small built-in light bulb or fibreoptic light) for airway illumination, and a curved or straight blade of various designs and lengths that can be hinged/interchanged or integral. Some types can be magnetic resonance imaging (MRI) compatible. This is a reusable device.

Other LARYNGOSCOPE, RIGID devices

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McGRATH 340-000-000
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2 deaths192 reports
McGRATH MAC 301-000-000
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2 recalls90 reports
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Karl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID
141 reports
n/a 8404AXC
Karl Storz GmbH & Co. KG · LARYNGOSCOPE, RIGID
108 reports
McGRATH 340-000-000
Covidien LP · LARYNGOSCOPE, RIGID
84 reports

All LARYNGOSCOPE, RIGID devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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