FDA Enforcement Class II Terminated

VitreQ 25G PFC Injection Needle-Ref: MD25.D01 GTIN: 8719214221386

Recall: Z-0850-2020 · Reported February 5, 2020

Enforcement

Recall Number
Z-0850-2020
Event ID
84661
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Vitreq Bv
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 5, 2020
Initiation Date
December 17, 2019
Classification Date
January 24, 2020
Termination Date
December 9, 2020
Address
Seggelant-Noord 2, N/A, Vierpolders, N/A, N/A, Netherlands

Description

VitreQ 25G PFC Injection Needle-Ref: MD25.D01 GTIN: 8719214221386

Reason

Microscopic tears of the sterile pouch may compromise sterility

Code Info

All lots

Distribution

Nationwide

Quantity

N/A