FDA · Medical devices ·
One-Piece Guedel Airway recall
Intersurgical Inc recalled One-Piece Guedel Airway on August 26, 2026 because of devices could potentially be occluded or partially occluded. It was sold nationwide.
Why it was recalled
Devices could potentially be occluded or partially occluded.
What's recalled
One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.
Quantity: 1,575 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Intersurgical Inc, East Syracuse, NY
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the states of CT, FL, IN, MI, OH & VA. - Status
- Ongoing
- Recall number
- Z-2953-2026
- Source
- U.S. Food and Drug Administration
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