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U.S. Department of Health and Human Services

Class 2 Device Recall UROLOGY PACK

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  Class 2 Device Recall UROLOGY PACK see related information
Date Initiated by Firm July 10, 2015
Date Posted September 03, 2015
Recall Status1 Terminated 3 on April 12, 2017
Recall Number Z-2592-2015
Recall Event ID 71721
510(K)Number K962652  
Product Classification Collector, urine, (and accessories) for indwelling catheter - Product Code KNX
Product UROLOGY PACK 4/CS
Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc.
.
Code Information Code:9001521 Lots: 141015699 exp. 11/30/15 141115980 exp. 12/31/15 150116560 exp. 2/28/16 150116560 exp. 2/28/16 150217271 exp. 2/28/16 150317613 exp. 4/30/16 150317616 exp. 4/30/16 150317615 exp. 4/30/16 150518646 exp. 5/31/16 150418301 exp. 5/31/16 150518647 exp. 5/31/16 150418302 exp. 5/31/16 150619387 exp. 6/30/16 
Recalling Firm/
Manufacturer
Customed, Inc
Calle Igualdad Final #7
Fajardo PR 00738
Manufacturer Reason
for Recall
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
FDA Determined
Cause 2
Packaging
Action Customed issued an "URGENT VOLUNTARY MEDICAL DEVICE RECALL" notification letter dated July 10, 2015 to all affected customers. The letter identified the product, problem, and actions to be taken by the customer.
Quantity in Commerce 352
Distribution Distributed Only in Puerto Rico.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = KNX and Original Applicant = CUSTOMED, INC.
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