FDA Enforcement Class II Terminated

AVID TruCustom PLASTIC BASIN PACK convenience kits, Item Code: MADN008-03

Recall: Z-0798-2018 · Reported March 7, 2018

Enforcement

Recall Number
Z-0798-2018
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 PLASTIC BASIN PACK convenience kits, Item Code: MADN008-03

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: 1203380 ,8/1/2018; 1203381, 8/1/2018; 1203382, 12/1/2018; 1211709, 12/23/2018

Distribution

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

Quantity

440