Intersurgical recalls green size 2 Guedel airways with model 1112080 due to potential small burrs that could cause airway blockage, irritation, or infection if inhaled.
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 green size 2 Guedel airways with model number 1112080 because small burrs inside could detach and be inhaled, leading to airway blockage or infection. This affects medical devices used during procedures like intubation.
The airway contains small burrs that can detach during use. If inhaled, these burrs may block the airway, cause irritation, inflammation, or infection in the respiratory tract.
Healthcare professionals using the airway device during medical procedures are most at risk. Patients receiving the device may also be affected if burrs become dislodged.
Look for green color, size 2, ISO 8.0, model number 1112080, or lot number 32414447 on the device. The UDI-DI (Case) is 05030267040698 and UDI-DI (Single Unit) is 5030267050659.
Identify the model number, color, size, and lot number to confirm if your device is recalled.
The recall indicates potential contamination with small burrs that could cause airway issues if inhaled, so it is not safe to use without checking the recall.
Check for green color, size 2, ISO 8.0, model number 1112080, or lot number 32414447 on the device.
The recall does not specify a remedy, so contact Intersurgical for guidance on next steps.
We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2275-2025 — Intersurgical Intersurgical Hello, I own a Intersurgical that is covered by recall Z-2275-2025 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.
