FDA Device recall Z-1706-2015
FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalation anesthesia on neonatal to adult patient…
- FDA Device
- Class I
- terminated
- Published 2015-06-17
On 2015-06-17 the FDA classified a Class I recall of FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalation anesthesia on neonatal to adult patient… by Maquet Cardiovascular Us Sales, citing in some Flow-i Anesthesia Systems, patient cassette can get dislodged which could result in gas leakage within the system internal circuit potentially leading to a stop in ventila….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1706-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-04-02 |
| Published | 2015-06-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Maquet Cardiovascular Us Sales |
| Distribution | AL, AZ, DC, FL, MI, MO, NJ, NY, OR, PA, TX, WV |
Product
FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalation anesthesia on neonatal to adult patient populations.
Reason
In some Flow-i Anesthesia Systems, patient cassette can get dislodged which could result in gas leakage within the system internal circuit potentially leading to a stop in ventilation.
Identifiers
| code_info | Article number 66 77 200 66 77 300 66 77 400 Serial Numbers 1058 1646 2034 2723 1059 1647 2095 2724 1060 1648…Article number 66 77 200 66 77 300 66 77 400 Serial Numbers 1058 1646 2034 2723 1059 1647 2095 2724 1060 1648 2186 2729 1172 1650 2554 2731 1201 1651 2555 2732 1202 1652 2556 2733 1204 1653 2557 2735 1224 1654 2558 2736 1225 1655 2559 2737 1226 1656 2560 2738 1277 1657 2561 2739 1280 1786 2562 2740 1281 1787 2613 2741 1282 1860 2714 2742 1545 1861 2716 2743 1546 2021 2719 2744 1643 2022 2720 2745 1644 2023 2721 2746 1645 2024 2722 2747 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1706-2015%22
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