M.D.L. S.r.l. recalls Aspirated Cyto-Histological Biopsy needle
- Recall date
- August 5, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2490-2021
- FDA classification
- Class II
- Brand / firm
- M.D.L. S.r.l.
- Sold / distributed
- Nationwide
Why it was recalled
Sterility assurance may be compromised.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Aspirated Cyto-Histological Biopsy needle
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