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U.S. Department of Health and Human Services

Class 2 Device Recall Major Laparotomy Pack

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 Class 2 Device Recall Major Laparotomy Packsee related information
Date Initiated by FirmJuly 10, 2015
Date PostedSeptember 03, 2015
Recall Status1 Terminated 3 on April 12, 2017
Recall NumberZ-2554-2015
Recall Event ID 71721
510(K)NumberK902031 
Product Classification General surgery tray (kit) - Product Code LRO
ProductMAJOR LAPAROTOMY PK 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 Catalog number:900036 Lots: 141015515 exp. 11/30/15 141015515 exp. 11/30/15 141216311 exp. 12/31/15 150116932 exp. 1/31/16 150116931 exp. 1/31/16 150116935 exp. 1/31/16 150116934 exp. 1/31/16 150116933 exp. 1/31/16 150217245 exp. 1/31/16 150217246 exp. 1/31/16 150217247 exp. 1/31/16 150317571 exp. 3/31/16 150317572 exp. 3/31/16 150317573 exp. 3/31/16 150317575 exp. 4/30/16 150317574 exp. 4/30/16 150418256 exp. 4/30/16 150418256 exp. 4/30/16 150418257 exp. 4/30/16 150418258 exp. 4/30/16 150418259 exp. 4/30/16 150518615 exp. 5/31/16 150518616 exp. 5/31/16 150518616 exp. 5/31/16 150519020 exp. 5/31/16 150519019 exp. 5/31/16 
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
ActionCustomed 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 Commerce1084 packs
DistributionDistributed Only in Puerto Rico.
Total Product Life CycleTPLC 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) Database510(K)s with Product Code = LRO
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