Magnolia Medical Technologies
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (1)
- MAGNOLIA MEDICAL TECHNOLOGIES, INC. FEI 3009976527 · WA
Recalls & enforcement
- Class IITerminated2021-11-02Due to an uptick of complaints associated with premature needle retraction of blood collection system.
- Class IITerminated2021-08-02Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Magnolia Medical Technologies — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10042579-magnolia-medical-technologies/
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