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

FDA Recall #Z-0854-2020 — Class II — December 17, 2019

Recall #Z-0854-2020 Date: December 17, 2019 Classification: Class II Status: Terminated

Product Description

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

Reason for Recall

Microscopic tears of the sterile pouch may compromise sterility

Recalling Firm

Vitreq Bv — Vierpolders, N/A

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

N/A

Distribution

Nationwide

Code Information

All lots

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

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