FDA Device recall Z-1877-2024
Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e
- FDA Device
- Class I
- ongoing
- Published 2024-06-12
On 2024-06-12 the FDA classified a Class I recall of Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e 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-1877-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-05-01 |
| Published | 2024-06-12 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Getinge Usa Sales |
| Distribution | CA, CO, IN, MO, OR, VA, WA |
Product
Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.
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 | Part Number 6682282; UDI/DI: 07325710000212: Serial Numbers: 17003 - 23454. |
|---|
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-1877-2024%22
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