FDA Enforcement Class II Terminated

NEURO SPINE PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

Recall: Z-2579-2015 · Reported September 9, 2015

Enforcement

Recall Number
Z-2579-2015
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

NEURO SPINE PACK 3/CS Used by medical staff to perform surgical procedures and 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

Code:9001300 Lots: 141015765 exp. 11/30/15 150116761 exp. 11/30/15 150418292 exp. 5/31/16 150518636 exp. 5/31/16

Distribution

Distributed Only in Puerto Rico.

Quantity

123 packs