Intersurgical recalls size 3 yellow Guedel airways with model 1113090 due to potential small burrs that could be inhaled, causing airway obstruction or infection. Affected units have specific model and lot numbers.
Potential contamination with small burrs, which if detach could be inhaled and result in potential complications such as airway obstruction, tissue irritation, inflammation and infection.
Intersurgical is recalling one-piece Guedel airways size 3 (model 1113090) because small burrs inside could detach and be inhaled, leading to airway blockage or infection. This is a serious risk for medical users handling the device.
Small burrs inside the airway device can detach during use and be inhaled. This may cause airway blockage, tissue irritation, inflammation, or infection if the burrs reach the airways.
Healthcare professionals using the Guedel airway during medical procedures are most at risk. Patients receiving the device could also be affected if burrs are inhaled.
Check for the yellow color, size 3, ISO 9.0, and model number 1113090. Affected units have lot number 32420657 or UDI-DI numbers starting with 05030267153961 or 5030267050680.
Look for the yellow color, size 3, ISO 9.0, model number 1113090, and lot number 32420657 on the device.
The recall states potential contamination with small burrs that could be inhaled, so it is not safe to use without checking the recall details.
The recall record does not specify a remedy, so contact Intersurgical directly for guidance.
Check for yellow color, size 3, ISO 9.0, model number 1113090, and lot number 32420657 or UDI-DI numbers starting with 05030267153961 or 5030267050680.
We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2276-2025 — Intersurgical Intersurgical Hello, I own a Intersurgical that is covered by recall Z-2276-2025 from Intersurgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
