Data Foundry

Medical device recalls 2024

Vaporizer Sevoflurane Maquet Filling — Class I medical device recall Z-1877-2024

Ongoing recall by Getinge Usa Sales Inc, reported 2024-06-12, distributed in CA, CO, IN, MO, OR, VA, WA. Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients o

Recall numberZ-1877-2024
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGetinge Usa Sales Inc, Wayne, NJ, United States
Recall initiated2024-05-01
Classified2024-05-31
Reported by FDA2024-06-12
DistributedCA, CO, IN, MO, OR, VA, WA
Countries outside the USAE, AT, AU, AW, BE, BG, BO, BR, CH, CL, CN, CR, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HK, HU, ID, IL, IN, IQ, IT, JO, JP, KE, KR, KW, LB, LT, MA, MX, MY, NI, NL, NO, OM, PE, PH, PK, PL, PT, PY, RO, RS, RU, SA, SE, SG, SK, TH, TN, TR, UA, VN, ZA
Quantity120 units
UPC / GTIN / UDI-DI07325710000212
Serial numbers17003, 23454
Model numbers6682282

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 for recall

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.

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-1877-2024. 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.