Medium risk Electronics & LightingClass II

Intersurgical Inc Recall

One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.

Updated June 15, 2026

Intersurgical Inc is recalling One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.. Hazard: Devices could potentially be occluded or partially occluded.

Is the Intersurgical Inc recalled? Yes. This product was recalled by FDA on June 15, 2026. Details below.

What is recalled

One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

Devices could potentially be occluded or partially occluded.

Brands affected

Source
FDA
Category
Electronics & Lighting
Recall ID
fda-Z-2953-2026
Classification
Class II
Recalled
June 15, 2026
Read the official notice

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