Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i… — Class II medical device recall Z-2860-2026
Ongoing recall by Maquet Critical Care AB, reported 2026-08-12, distributed nationwide. Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver
| Recall number | Z-2860-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Critical Care AB, Solna, Sweden |
| Recall initiated | 2026-06-24 |
| Classified | 2026-08-03 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 07325710001318, 07325710001349, 07325710001363, 07325710009765, 07325710010457, 07325710010617, 07325710010624, 07325710010631 |
Product
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900
Reason for recall
Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperative awareness.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2860-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.