FDADecember 17, 2019device

VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Microscopic tears of the sterile pouch may compromise sterility

What to do

FDA enforcement status: Terminated

Brands named

vitreq bvvitreq

UPCs

8719214221485

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485 — Recall Details · AllClear