FDA Enforcement Class II Terminated

AVID TruCustom GENERAL PACK convenience kits, Item Code: LGHM041-06 and LGHM041-08

Recall: Z-0789-2018 · Reported March 7, 2018

Enforcement

Recall Number
Z-0789-2018
Event ID
79162
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Avid Medical, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
March 7, 2018
Initiation Date
June 22, 2017
Classification Date
February 28, 2018
Termination Date
October 12, 2018
Address
9000 Westmont Dr, N/A, Toano, VA, 23168-9351, United States

Description

AVID TruCustom GENERAL PACK convenience kits, Item Code: LGHM041-06 and LGHM041-08

Reason

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Code Info

Lot, Expiration Date: 1213947, 7/1/2019; 1216720, 10/1/2018; 1221271, 8/1/2017

Distribution

Distributed in 10 states: IL, KY, LA, MA, MO, NY, OH, TX, VA, WI.

Quantity

630