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Vitreq Bv recalls VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485
Recalled February 5, 2020 · FDA recall Z-0854-2020 · Vitreq Bv
Hazard
Microscopic tears of the sterile pouch may compromise sterility · FDA Class II
Units
N/A
Sold at
Nationwide
Description
Microscopic tears of the sterile pouch may compromise sterility
Product
VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485
Manufacturer(s)
Vitreq Bv
Made in
Netherlands
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →