Use caution Medical device recall · FDA · Published October 20, 2025

Mindray Sevoflurane V90 Vaporizer Recall: Potential Anesthesia Leakage Risk

Mindray recalls Sevoflurane V90 Electronic Vaporizers with A9 Anesthesia System due to potential anesthesia leakage. Affected units have specific serial numbers and part numbers.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0720-2026Medical device Mindray ›

Use caution until it’s fixed

Potential for anesthesia leakage.

Take action

Contact the company

Recalling firmMindray DS USA, Inc. dba Mindray North America800 Macarthur Blvd · Mahwah, NJ 07430-2001

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/51039-mindray-sevoflurane-v90-vaporizer-recall-potential-anesthesia-leakage-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/51039-mindray-sevoflurane-v90-vaporizer-recall-potential-anesthesia-leakage-risk · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0720-2026

Cite this page

“Mindray Sevoflurane V90 Vaporizer Recall: Potential Anesthesia Leakage Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/51039-mindray-sevoflurane-v90-vaporizer-recall-potential-anesthesia-leakage-risk. Based on FDA recall #Z-0720-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0720-2026%22&limit=1).

The FDA announced on Oct. 20, 2025, that Mindray DS USA Inc. dba Mindray North America is recalling Sevoflurane (SEVO) V90 Electronic Vaporizers with the A9 Anesthesia System due to a potential for anesthesia leakage. The recall affects 148 units distributed worldwide.

How to tell if you have it

Brand: Mindray
Product: Sev E_Vap (Safety Filling adapter), Part Number: 115-066756-00, DI: 06936415975777
Product: Exchange Sev E_Vap (Safety Filling adapter), Part Number: E115-066756-00, DI: 06936415975777
Units affected: 148

The hazard

The recall cites a potential for anesthesia leakage from the device. The A9 Anesthesia System utilizes V90 electronic vaporizers for anesthetic agent delivery.

Context

GovInfoNow's records show Mindray DS USA Inc. dba Mindray North America has 13 other recalls on record since July 14, 2017. Other recent recalls of similar products include Draeger Vapor 3000 Anesthetic Vaporizer Recall (Nov. 24, 2025), Draeger Vapor 2000 Anesthetic Vaporizer Recall (Nov. 24, 2025) and Medline Medical Kits Recall (Dec. 16, 2025).

How to tell if you have this one

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.

Brand
Mindray
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide distribution in the states of California, Florida, Georgia, Kentucky, Maryland, Mississippi, Missouri, New Jersey, Puerto Rico, Texas, Washington, West Virginia and the country of Canada.

Recall number	Product, codes & lots	Quantity
Z-0720-2026	Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: The Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. The A9 Anesthesia System utilizes V90 electronic vaporizers for anesthetic agent delivery.; 1. Part Number: 115-066756-00; DI: 06936415975777; Serial Numbers: AH6A45000871, AH6A45000880, AH6A45000881, AH6A46000929, AH6A46000931, AH6A46000944, AH6A47001200, AH6A44000657, AH6A44000658, AH6A44000661, AH6A44000664, AH6A44000677, AH6A44000678, AH6A44000680, AH6A44000768, AH6A44000778, AH6A46000925, AH6A46000927, AH6A46000928, AH6A46000935, AH6A46000937, AH6A46001114, AH6A47001159, AH6A47001164, AH6A47001174, AH6A47001201, AH6A45000872, AH6A46000932, AH6A46000939, AH6A46000940, AH6A47001196, AH6A47001202, AH6A47001207, AH6A47001215, AH6A46001102, AH6A46001111, AH6A46001116, AH6A47001160, AH6A47001161, AH6A47001163, AH6A47001165, AH6A47001166, AH6A47001167, AH6A47001178, AH6A46001097, AH6A46001117, AH6A44000645, AH6A44000647, AH6A44000648, AH6A44000651, AH6A44000655, AH6A44000656, AH6A44000659, AH6A44000660, AH6A44000662, AH6A44000684, AH6A44000686, AH6A44000687, AH6A44000688, AH6A44000690, AH6A44000691, AH6A44000695, AH6A44000696, AH6A44000698, AH6A44000700, AH6A44000702, AH6A44000703, AH6A44000770, AH6A44000776, AH6A46001090, AH6A46001109, AH6A46001118, AH6A47001171, AH6A47001176, AH6A44000771, AH6A44000772, AH6A45000815, AH6A45000819, AH6A45000821, AH6A45000822, AH6A45000824, AH6A45000825, AH6A45000829, AH6A45000832, AH6A45000834, AH6A45000835, AH6A45000868, AH6A45000869, AH6A45000870, AH6A45000873, AH6A45000874, AH6A45000875, AH6A45000876, AH6A45000877, AH6A45000878, AH6A45000882, AH6A45000883, AH6A45000884, AH6A46000926, AH6A46000930, AH6A46000936, AH6A46000943, AH6A44000779, AH6A44000674, AH6A44000692, AH6A44000777, AH6A45000879, AH6A47001170, AH6A44000765, AH6A44000769, AH6A47001175, AH6A28000535, AH6A46000918, AH6A46000923, AH6A46000924, AH6A46000934, AH6A46000938, AH6A46001091, AH6A46001093, AH6A46001099, AH6A46001100, AH6A46001101, AH6A46001103, AH6A46001104, AH6A46001107, AH6A46001108, AH6A46001110, AH6A46001113, AH6A47001177, AH6A44000679, AH6A44000683, AH6A44000689, AH6A44000697, AH6A44000649, AH6A44000650, AH6A44000652, AH6A44000676, AH6A44000681, AH6A44000682, AH6A44000699, AH6A44000704, AH6A44000766, AH6A44000773, AH6A44000775, AH6A44000780, AH6A47001216, AH6A44000693. 2. Part Number: E115-066756-00; DI: 06936415975777; Serial Number: AH6A45000885.	148 units
Z-0721-2026	Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Iso E_Vap. (Safety Filling adapter), Part Number 115-066758-00. 2. Exchange Iso E_Vap. (Safety Filling adapter), Part Number E115-066758-00. Product Description: The Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. The A9 Anesthesia System utilizes V90 electronic vaporizers for anesthetic agent delivery.; 1. Part Number 115-066758-00; DI 06936415975753; Serial Numbers: AH6B44000714, AH6B44000719, AH6B44000722, AH6B44000724, AH6B44000733, AH6B44000734, AH6B44000782, AH6B45000836, AH6B45000837, AH6B45000840, AH6B45000844, AH6B45000858, AH6B44000717, AH6B44000786, AH6B44000785, AH6B44000788, AH6B45000859, AH6B44000671, AH6B44000673, AH6B44000705, AH6B44000706, AH6B44000707, AH6B44000708, AH6B44000709, AH6B44000710, AH6B44000711, AH6B44000712, AH6B44000713, AH6B44000715, AH6B44000716, AH6B44000718, AH6B44000723, AH6B44000725, AH6B44000726, AH6B44000727, AH6B44000728, AH6B44000729, AH6B44000730, AH6B44000731, AH6B44000783, AH6B44000787, AH6B44000790, AH6B45000839, AH6B45000854, AH6B44000732, AH6B45000856, AH6B44000789, AH6B45000842, AH6B45000841, AH6B45000845, AH6B45000850, AH6B45000852, AH6B45000853. 2. Part Number E115-066758-00; 06936415975753; Serial Number: AH6B44000672.	54 units

Based on the official FDA remedy

What to do — step by step

Check Device Model
Look for the model name 'Sev E_Vap' or part numbers 115-066756-00 or E115-066756-00 on the device.
Contact Manufacturer
Reach out to Mindray North America for details on the specific serial numbers and part numbers that are affected.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 11 states.

FDA distribution: “Worldwide - US Nationwide distribution in the states of California, Florida, Georgia, Kentucky, Maryland, Mississippi, Missouri, New Jersey, Puerto Rico, Texas, Washington, West Virginia and the country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Florida, Georgia, Kentucky, Maryland, Mississippi, Missouri, New Jersey, Puerto Rico, Texas, Washington, West Virginia.

Recall timeline

FDA published this recall 44 days after the firm started it.

Oct 20, 2025Firm started the recall
Nov 26, 2025FDA classified it Class II
Dec 3, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What should I do if I have this device?

Contact Mindray North America to confirm if your device is affected and follow their instructions for next steps.

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Link to this recall

<a href="https://govinfonow.com/recall/51039-mindray-sevoflurane-v90-vaporizer-recall-potential-anesthesia-leakage-risk">Mindray Sevoflurane V90 Vaporizer Recall: Potential Anesthesia Leakage Risk (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-0720-2026 (October 20, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0720-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.