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U.S. Department of Health and Human Services

Class 2 Device Recall OPHTHALMIC PACK

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  Class 2 Device Recall OPHTHALMIC 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-2612-2015
Recall Event ID 71721
Product Classification Eye tray - Product Code OJK
Product OPHTHALMIC PACK 6/CS
Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc.
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Code Information Code:9001780 Lots: 141015756 exp. 9/30/16 141216419 exp. 12/31/16 150116978 exp. 2/28/16 150317700 exp. 4/30/16 150317701 exp. 4/30/16 150317702 exp. 4/30/16 150518592 exp. 6/30/16 150518593 exp. 6/30/16 150518594 exp. 6/30/16 150518594 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 546
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.
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