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U.S. Department of Health and Human Services

Class 3 Device Recall Episeal wound closure strips

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  Class 3 Device Recall Episeal wound closure strips see related information
Date Initiated by Firm February 07, 2012
Date Posted April 17, 2012
Recall Status1 Terminated 3 on July 10, 2013
Recall Number Z-1421-2012
Recall Event ID 61403
Product Classification Tape and bandage, adhesive - Product Code KGX
Product Sterile wound closure strips, packaged as follows:
DeRoyal EPISEAL, Wound Closure Strips, REF 46-202, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-203, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-204, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-206, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-212, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-213, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-214, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-215, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849

DeRoyal EPISEAL, Wound Closure Strips, REF 46-216, STERILE R, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849
Code Information REF 46-202, Lot Number: 346935; REF 46-203, Lot Numbers: 345495, 362263; REF 46-204, Lot Numbers: 350142, 344274; REF 46-206, Lot Numbers: 342708, 2360103; REF 46-212, Lot Numbers: 352631, 345230; REF 46-213, Lot Number: 350152; REF 46-214, Lot Numbers: 344278, 345232; REF 46-215, Lot Number: 345242; REF 46-216, Lot Numbers: 585961, 350276
Recalling Firm/
Manufacturer
Deroyal Industries, Inc. Lafollette
1501 East Central Ave
La Follette TN 37766-2892
For Additional Information Contact Tracy Edmundson
865-362-2334
Manufacturer Reason
for Recall
Packages of Episeal wound closure strips and surgical kits containing them were recalled because the adhesive backing on Episeal wound closure strips may not release from the backing rendering the product unusable.
FDA Determined
Cause 2
Nonconforming Material/Component
Action DeRoyal Industries sent a Recall of Episeal Wound Closure Strip letter dated February 7, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Customers were instructed to take the following action: 1. Please identify and quarantine any affected inventory using the product and lot numbers listed above. 2. Render affected product unusable, destroy and discard according to your facilitys guidelines. 3. If you are a distributor, forward this recall to any of your end users that may have affected product or provide us with the list and we will contact them. 4. Please complete the enclosed Notice of Destruction form, indicating the affected products you found in your inventory and destroyed. PLEASE COMPLETE AND RETURN THIS FORM EVEN IF YOU NO LONGER HAVE THE PRODUCT IN INVENTORY. Return this form by fax (865-362-3716) or email (recalls@deroyal.com) within two weeks of the date of this letter. DeRoyal will use your response on the Notice of Destruction form to send replacements as soon as they become available. If you have questions or need assistance with the recall, please contact DeRoyal Customer Support at 1-800-251-9864. We apologize for inconvenience this may cause you
Quantity in Commerce 126,720 units
Distribution Worldwide Distribution -- USA (nationwide)
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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