FDA Device recall Z-1074-2025
Vaporizer Sevoflurane, Quik-Fil
- FDA Device
- Class I
- ongoing
- Published 2025-02-19
On 2025-02-19 the FDA classified a Class I recall of Vaporizer Sevoflurane, Quik-Fil by Getinge Usa Sales, citing sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Pote….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1074-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-01-15 |
| Published | 2025-02-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Getinge Usa Sales |
| Distribution | CT, KY |
Product
Vaporizer 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.
Reason
Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema and/or severe hypocalcemia, blistering, superficial ulceration, and/or hypomagnesemia.
Identifiers
| code_info | Model Number: 6682285. UDI-DI: 07325710001141. Serial Numbers: 3761, 7635, 7633, 7630, 7632, 7631. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1074-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.