Mindray recalls Sevoflurane E_Vap Safety Filling Adapters for A9 Anesthesia Systems due to potential high anesthetic output causing patient drowsiness or neurological issues. Affected units have specific serial numbers.
V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention
Mindray is recalling Sevoflurane E_Vap Safety Filling Adapters used with A9 Anesthesia Systems. The adapters may cause higher anesthetic output than set, leading to patient drowsiness or neurological problems after surgery. This is serious enough to require immediate action.
The safety filling adapter may have an incomplete seal, causing the anesthetic output to exceed the set concentration. This can lead to patients inhaling too much anesthetic, causing drowsiness or neurological problems like memory issues after surgery.
Healthcare professionals using the A9 Anesthesia System with the recalled adapters are affected. Patients undergoing anesthesia with these systems are at risk of drowsiness or neurological issues.
Check for serial numbers: AH6A28000471, AH6A24000202, AH6A28000474, AH6A27000378, AH6A28000466, AH6A24000195, AH6A28000457, AH6A25000237, AH6A28000426, AH6A24000199, AH6A24000207. The product is used with the A9 Anesthesia System.
Immediately stop using the recalled Sevoflurane E_Vap Safety Filling Adapter with the A9 Anesthesia System.
The recalled adapter is the Sevoflurane E_Vap Safety Filling Adapter with part number 115-066756-00.
Affected units have serial numbers: AH6A28000471, AH6A24000202, AH6A28000474, AH6A27000378, AH6A28000466, AH6A24000195, AH6A28000457, AH6A25000237, AH6A28000426, AH6A24000199, AH6A24000207.
Immediately stop using it and contact Mindray for further instructions.
We’ve drafted a message you can send Mindray to request your refund or repair — edit it as you like.
Subject: Recall Z-2950-2024 — Mindray Mindray Hello, I own a Mindray that is covered by recall Z-2950-2024 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.
