Reported Dec 3, 2025 · Ongoing
Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap.…
Mindray DS USA, Inc. dba Mindray North America
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Mindray DS USA, Inc. dba Mindray North America · 800 Macarthur Blvd · Mahwah, NJ · 07430-2001
Is this the product you have?
- Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System
- Labeled as the following1. Sev E_Vap. (Safety Filling adapter)
- Part Number115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter)
- Part NumberE115-066756-00
- Product DescriptionThe 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
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published 115-066756-00— — 06936415975777DI: 06936415975777 E115-066756-00Serial 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. — 06936415975777DI: 06936415975777 — Serial Number: AH6A45000885. - Amount recalled
- 148 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Potential for anesthesia leakage.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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