Vaporizer Sevoflurane, MAQUET filling 6886601Recalls & reported problems
Maquet Critical Care AB · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
10 other recalls cover devices cleared under the same FDA submission (K191027); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Dec 9, 2021Class IOpen, Classified
A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides and metal halides) has been discovered that may result in inhalation and/or skin exposure of hydrogen fluoride.
Z-0468-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K191027. One submission often covers many models, so check the product and lot details in each record.
- Z-2860-2026 · Jun 24, 2026 · Open, ClassifiedFlow 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
- Z-1074-2025 · Jan 15, 2025 · Open, ClassifiedVaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.
- Z-1877-2024 · May 1, 2024 · Open, ClassifiedVaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.
- Z-0960-2023 · Dec 22, 2022 · Open, ClassifiedGetinge Flow-c Anesthesia System, Part No. 6887700
- Z-0961-2023 · Dec 22, 2022 · Open, ClassifiedGetinge Flow-e Anesthesia System, Part No. 6887900
- Z-0959-2023 · Dec 22, 2022 · Open, ClassifiedGetinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 Flow-i C40, Part no. 6677400
- Z-0422-2023 · Nov 7, 2022 · Open, ClassifiedFlow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System (Product Code 6887900)
- Z-1278-2022 · May 2, 2022 · TerminatedFlow-c Anesthesia System : intended for use in administering anesthesia while controlling the entire ventilation of patient Product Code/REF Number: 6887700
- Z-1279-2022 · May 2, 2022 · TerminatedFlow-e Anesthesia System : Intended for use in administering anesthesia while controlling the entire ventilation of patient Product Code/REF Number: 6887900
- Z-1181-2021 · Jan 29, 2021 · TerminatedAnesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in
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- Aisys CS2Datex-Ohmeda Inc · Gas-machine, anesthesia5 recalls2,048 reports
- Carestation 620 A1Datex-Ohmeda Inc · Gas-machine, anesthesia2 recalls2,015 reports
- Avance CS2Datex-Ohmeda Inc · Gas-machine, anesthesia6 recalls1,540 reports
- Flow-c Anesthesia System 6887700Maquet Critical Care AB · Gas-Machine, Anesthesia6 recalls72 reports
- FLOW-i C20 6677200Maquet Critical Care AB · Gas-Machine, Anesthesia4 recalls99 reports
- Flow-e Anesthesia System 6887900Maquet Critical Care AB · Gas-Machine, Anesthesia5 recalls19 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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