Assurance Infusion recalls QUADMIX in 1 mL vial Assurance Infusion (713)-533-8800
- Recall date
- December 20, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0763-2020
- FDA classification
- Class II
- Brand / firm
- Assurance Infusion
- Sold / distributed
- Nationwide within the United States
Why it was recalled
Lack of sterility assurance.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
QUADMIX in 1 mL vial Assurance Infusion (713)-533-8800
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