Mindray recalls Desflurane E_Vap (Saf-T-Fill) used with A9 Anesthesia System due to potential over-delivery of anesthetic. Patients may experience drowsiness or neurological issues if overdose occurs.
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 Desflurane E_Vap (Saf-T-Fill) used with the A9 Anesthesia System because a faulty component may cause the anesthetic to be delivered in higher concentrations than set. This could lead to symptoms like drowsiness or neurological problems after surgery.
The vaporizer's seal may become incomplete, causing the anesthetic to be delivered in higher concentrations than intended. This can lead to patients inhaling too much anesthetic, resulting in symptoms like drowsiness or neurological issues after surgery.
Patients undergoing anesthesia using this specific device are most at risk. Healthcare providers using the A9 Anesthesia System with the recalled Desflurane E_Vap may need to take extra care.
Check for the part number 115-066759-00 or serial numbers listed in the recall notice. The product is used with the A9 Anesthesia System and sold by Mindray North America.
Look for serial numbers starting with AH6C25000254 or similar as listed in the recall notice.
If you use this device, contact your healthcare provider to discuss potential risks and next steps.
The recalled device is Desflurane E_Vap (Saf-T-Fill) used with the A9 Anesthesia System, with part number 115-066759-00.
Patients may experience drowsiness, vertigo, or neurological issues like hypomnesia and inattention after surgery.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Mindray to request your refund or repair — edit it as you like.
Subject: Recall Z-2952-2024 — Mindray Mindray Hello, I own a Mindray that is covered by recall Z-2952-2024 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.
