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U.S. Department of Health and Human Services

Class 2 Device Recall Scorpio Adjustable Femoral A/P Sizing Guide

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 Class 2 Device Recall Scorpio Adjustable Femoral A/P Sizing Guide see related information
Date Posted January 19, 2011
Recall Status1 Terminated on July 31, 2013
Recall Number Z-0927-2011
Recall Event ID 56931
Product Classification Orthopedic manual surgical instrument - Product Code LXH
Product Scorpio Adjustable Femoral A/P Sizing Guide Assembly;
non-sterile instruments; Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430; A subsidiary of Stryker Corporation

The A/P sizer is designed to set the desired external rotation and to provide adjustment of the anterior/posterior position when needed.
Code Information Catalog Number 8000-0313
Lot numbers: RD2M081 RD2MO80 RD2N006 RD2N006E RD2L054 RD2M080E RD2S005X1 RD2S005 RD2S060 RD2N006S RD2S060S RD2S059 RD2V064 RD2V063 RD2V067 RD2V068 RD2V067A RD2V064E RD2V068S RD3A027 RD3A027M RD2V067M RD3A011 RD3A010 RD3A010A RD2VO68M RD3A011H RD3A009 RD2V068H RD3A027H RDA070H RD3A069 RD3A069H RD3A070 RD3L033 RD3N205 RD3N205X1 RD3S020 RD3S094 RD3V086
Recalling Firm/
Stryker Howmedica Osteonics Corp.
325 Corporate Drive
Mahwah NJ 07430
For Additional Information Contact Ms. Colleen O'Meara
Manufacturer Reason
for Recall
Stryker Orthopaedics has become aware that there is a potential for the shoulder screw on the Scorpio Sizing Guide (the "Sizing Guide") to disassociate from the main body of the instrument.
FDA Determined
Cause 2
Device Design
Action Stryker Orthopaedics sent an 'Urgent Update Product Recall' letter dated December 30, 2010, along with Product Acknowledgement forms to all customers (US and international). The letter described the product, problem and action to be taken by the customers. The customers were asked to complete and return the PRODUCT RECALL ACKNOWLEDGMENT FORM within five (5) days via fax at 201-831-6069; contact the hospitals in their territory that have the affected product to arrange return of the product; and return the affected product to the attention of Regulatory Compliance, Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. If you have any questions, feel free to contact the Manager, Divisional Regulatory Compliance at (201) 972-2100 or the Associate Product Manager, Knee Marketing Team, at (201) 831-5028.
Quantity in Commerce 237 units
Distribution Worldwide distribution: USA and countries including: Australia, Brazil, China, Columbia, France, Greece, India, Italy, Korea, Poland, Singapore, South Africa, and United Kingdom.
Total Product Life Cycle TPLC Device Report

1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.