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U.S. Department of Health and Human Services

Class 2 Device Recall Osteoraptor Suture Anchor

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  Class 2 Device Recall Osteoraptor Suture Anchor see related information
Date Initiated by Firm August 06, 2013
Date Posted September 17, 2013
Recall Status1 Terminated 3 on April 20, 2016
Recall Number Z-2222-2013
Recall Event ID 66037
510(K)Number K082215  
Product Classification Staple, fixation, bone - Product Code JDR
Product OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White; Part Number: 72201991

Biodegradable suture anchor
Code Information 50272333 50272460 50272749 50273092 50274145 50274574 50277104 50277531 50278113 50281660 50283022 50283200 50283850 50285450 50287132 50290044 50290336 50292248 50293720 50295817 50298408 50301689 50302077 50305597 50307616 50307617 50307618 50307663 50308924 50308925 50308926 50309406 50309508 50310779 50311755 50312497 50314731 50316178 50316439 50317760 50318970 50320251 50320672 50321643 50321930 50322929 50324017 50325608 50326698 50327820 50329812 50331690 50332905 50334815 50336529 50339426 50340626 50341618 50343004 50343606 50344261 50344616 50346627 50350512 50351012 50351958 50353154 50353603 50354094 50355980 50356986 50358573 50359120 50360006 50360806 50361757 50362646 50363764 50364908 50364913 50364914 50370384 50372334 50372727 50372893 50374260 50375049 50375595 50378705 50378911 50379639 50380393 50380529 50383897 50384594 50385078 50385697 50387883 50388027 50388266 50389118 50390497 50392265 50394521 50395089 50395537 50397272 50397703 50399280 50400568 50401030 50401758 50402612 50403120 50403717 50404750 50405222 50406196 50407002 50407567 50407939 50408700 50409823 50411054 50412275 50413141 50414235 50415253 50415494 50416128 50416525 50417009 50417383 50418000 50418498 50419235 50421349 50423113 50423434 50425116 50426665 50426939 50427505 50429270 50430180 50431376 50433037 50433126 50434434 50435065 50435511 50438086 50438658 50439570 50440210 50441218 50442032 50444061 50444660 50445139 50445312 50445544 50445545 50446349 50447136 50448057 50449021 50449978 50449979 50449981 50449983 50449984 50449985 50450604 50450947 50451941 50452039 50453146 50453803 50454293 50454688 50455482 50455623 50456054 50456340 50456908 50458605 50460096 50460239 50461691 50462794 50463457 50466682 
Recalling Firm/
Manufacturer		 Smith & Nephew, Inc. Endoscopy Division
150 Minuteman Drive
Andover MA 01810-1031
For Additional Information Contact Albert A. Pytka
978-749-1073
Manufacturer Reason
for Recall		 Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
FDA Determined
Cause 2		 Packaging
Action Smith&Nephew sent an Urgent Product Recall Notification letter dated August 6, 2013, via Federal Express to all affected customers. Addendum customer letters for 4 additional part numbers were sent via Federal Express on August 19, 2013, The letters identified the product, the problem, and the action to be taken by the customer. Customers were asked to inspect their inventory, locate unused devices and quarantine them. Customers were also asked to complete the last three columns in the inventory Return Certification form indicating the quantities that need to be returned, and include their contact information in the spaces provided. Customers were instructed to contact Smith & Nephew's Demo Service Departmentat 800-343-5717 for a Return Authorization (RA#), and provide the information response form. Replacement product would be provided. For questions regarding this recall call 978-749-1073.
Quantity in Commerce 22879 US
Distribution Worldwide Distribution - USA (nationwide) Canada, Europe: Austria, Belgium, Cyprus, Czech Republic, Denmark, Germany, Greece, Finland, France, Italy, Ireland, Luxembourg, Netherlands, Norway, Poland, Portugal, Russia, Slovenia, Spain, Sweden, Switzerland, Turkey, Ukraine and United Kingdom, Asia-pacific: Australia, China, Dubai, Hong Kong, India, Japan, Malaysia, New Zealand, Philippines, Sri Lanka, Singapore, South Korea, Taiwan, Thailand, Argentina, Bermuda, Brazil, Chile, Colombia, Costa Rica, Israel, Mexico, Puerto Rico, South Africa, and Venezuela.
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 = JDR and Original Applicant = SMITH & NEPHEW INC., ENDOSCOPY DIVISION
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