Intersurgical recalls specific light green oropharyngeal airway devices due to potential occlusion. Affected units include certain lot numbers and sizes. Consumers should check their device details and contact Intersurgical for guidance.
Devices could potentially be occluded or partially occluded.
Intersurgical is recalling light green One-Piece Guedel Airway devices (size 000, ISO 3.5) because they might become partially blocked. This could cause breathing difficulties during medical procedures if the device isn't properly clear.
The airway devices could become partially blocked during use, which might interfere with maintaining a clear airway for patients. This is a potential risk during medical procedures where the device is used to keep an airway open.
Healthcare professionals using these airway devices in medical settings are most at risk. Patients receiving airway care with the recalled devices could also be affected.
Check for the light green color, size 000, ISO 3.5, and the specific lot numbers listed in the recall notice. The device is a single-use oropharyngeal airway device.
Look for the light green color, size 000, ISO 3.5, and the listed lot numbers on the device packaging or label.
The devices could potentially be occluded or partially occluded, which might interfere with maintaining a clear airway during medical procedures.
Check the device details against the recall list. If you have the affected model, contact Intersurgical for further instructions.
The recall is due to a potential risk of partial blockage, which could affect airway management during medical procedures.
We’ve drafted a message you can send Intersurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2953-2026 — Intersurgical Intersurgical Hello, I own a Intersurgical that is covered by recall Z-2953-2026 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.
