FDA Enforcement Class II Terminated

SUTURE REMOVAL KIT CUSTOMED 100/CS Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

Recall: Z-2549-2015 · Reported September 9, 2015

Enforcement

Recall Number
Z-2549-2015
Event ID
71721
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Customed, Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
September 9, 2015
Initiation Date
July 10, 2015
Classification Date
September 3, 2015
Termination Date
April 12, 2017
Address
Calle Igualdad Final #7, N/A, Fajardo, PR, 00738, United States

Description

SUTURE REMOVAL KIT CUSTOMED 100/CS Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

Reason

Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Code Info

Catalog number: 900010 Lots: 141015851 exp. 10/31/2015 150116710 exp.1/31/2016 150117001 exp.2/28/2016 150317560 exp.3/31/2016 150317560 exp.3/31/2016 150418252 exp.5/31/2016 150418252 exp.5/31/2016 150518605 exp.5/31/2016 150518605 exp.5/31/2016

Distribution

Distributed Only in Puerto Rico.

Quantity

20200 kits