Vitreq Bv recalls VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423
- Recall date
- December 17, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0851-2020
- FDA classification
- Class II
- Brand / firm
- Vitreq Bv
- Sold / distributed
- Nationwide
Why it was recalled
Microscopic tears of the sterile pouch may compromise sterility
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423
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