Mindray recalls Sevoflurane V90 Electronic Vaporizers with A9 Anesthesia System due to potential anesthesia leakage. Affected units have specific serial numbers and part numbers.
Potential for anesthesia leakage.
Mindray is recalling Sevoflurane V90 Electronic Vaporizers with the A9 Anesthesia System because they may leak anesthesia. This could pose a risk during medical procedures if the device isn't properly sealed.
The device may leak anesthetic gas during use, which could lead to unintended exposure for patients or staff. This leakage might occur if the safety filling adapter is not properly sealed or if the device is used incorrectly.
Healthcare professionals using anesthesia equipment for patients are most at risk. The recall affects specific models with serial numbers and part numbers listed in the notice.
Check for the model name 'Sev E_Vap' or part numbers 115-066756-00 or E115-066756-00. Affected units have specific serial numbers listed in the recall notice.
Look for the model name 'Sev E_Vap' or part numbers 115-066756-00 or E115-066756-00 on the device.
Reach out to Mindray North America for details on the specific serial numbers and part numbers that are affected.
The recall states there is a potential for anesthesia leakage, but it does not specify that the device is unsafe if used correctly. The risk depends on proper sealing and usage.
Check for the model name 'Sev E_Vap' or part numbers 115-066756-00 or E115-066756-00. Affected units have specific serial numbers listed in the recall notice.
Contact Mindray North America to confirm if your device is affected and follow their instructions for next steps.
We’ve drafted a message you can send Mindray to request your refund or repair — edit it as you like.
Subject: Recall Z-0720-2026 — Mindray Mindray Hello, I own a Mindray that is covered by recall Z-0720-2026 from Mindray. 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.
