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U.S. Department of Health and Human Services

Class 1 Device Recall Customed

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  Class 1 Device Recall Customed see related information
Date Initiated by Firm May 20, 2014
Date Posted August 29, 2014
Recall Status1 Terminated 3 on August 14, 2017
Recall Number Z-2325-2014
Recall Event ID 68536
Product Classification General surgery tray (kit) - Product Code LRO
Product CYSTO TUR PACK- -
(1) UTILITY BOWL 32oz LIF
(1) SPECIMEN CUP WITH CAP 4oz LIF
(1 0) GAUZE SPONGE 4" X 4" 12PL Y LIF
(4) ABSORBENT TOWELS 15" X 20" LIF
(1) CYSTOSCOPY 'T' DRAPE 60" X 87" X 35" SMS STD LIF
(2) GOWN IMPERVIOUS EXTRA REINFORCED X-LARGE LIF
(2) LEGGINS WITH 7" CUFF 30" X 42" LIF
(1) TABLE COVER REINFORCED 44" X 78" LIF
(1) UNDERBUTTOCK DRAPE WITH POUCH 44" X 35" LIF
(1) SYRINGE 60ML SLUER SLIP WITHOUT NEEDLE LIF
(1) TUR Y SET 81 "2.1 M REGULAR CLAM
(4) GAUZE SPONGES 4" X 4" 12 PLY XRD L/F
EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents
Code Information Product code 900-430, 29 lots: 110020453 110030667 110051146 111030671 111040897 111061672 111071814 111082217 111092389 111102877 111113116 111123253 112010174 112030874 112041411 112072872 112083431 113015513 113015697 113036365 113047211 113057626 113078328 113088864 113109841 131110304 140111229 140312164 140412467 
Recalling Firm/
Manufacturer		 Customed, Inc
Calle Igualdad Final #7
Fajardo PR 00738
For Additional Information Contact Rosemari Melendez
787-622-5151 Ext. 7540
Manufacturer Reason
for Recall		 Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.
FDA Determined
Cause 2		 Package design/selection
Action Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit. Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540
Quantity in Commerce 29 lots; 870 units (multiple units per lot)
Distribution Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.
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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