FDA Medical devices recall ·
Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System recall
- Recall number
- Z-0720-2026
- Date
- (initiated October 20, 2025)
- Company / brand
- Mindray North America
800 Macarthur Blvd, Mahwah, NJ, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 148 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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.
Why was it recalled?
Potential for anesthesia leakage.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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, AH6A4
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: California Florida Georgia Kentucky Maryland Missouri Mississippi New Jersey Puerto Rico Texas Washington West Virginia
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0720-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.