Vitreq Bv recalls (1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF: BF20.D52 GTIN: 8…
- Recall date
- December 17, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0848-2020
- 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
(1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF: BF20.D52 GTIN: 8719214221102
Get recall alerts
Free email alert whenever Vitreq Bv has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Vitreq Bv