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U.S. Department of Health and Human Services

Class 2 Device Recall OSS Letson Proximal Femoral Trial 7 cm

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 Class 2 Recall
OSS Letson Proximal Femoral Trial 7 cm
see related information
Date Posted June 29, 2009
Recall Status1 Terminated on October 08, 2010
Recall Number Z-1529-2009
Recall Event ID 51980
Premarket Notification
510(K) Numbers
K002757  K043547 
Product Classification Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer - Product Code KRO
Product Biomet OSS Letson Proximal Femoral Trial 7 cm resection/left, stainless steel, Biomet Orthopedics, Inc., Warsaw, IN; REF 32-472089. A non-powered, orthopedic manual surgical instrument for use with other devices in orthopedic surgery.
Code Information All lots. Lots 063960, 115390, 115460, 197210, 206280, 238310, 252780, 397280, 405110, 444100, 444110, 488440, 506470, 536100, 632470, 635860, 641450, 721420, 775240, 793530, 797790, 839640, 849140, 892440, 894240 and 895840.
Recalling Firm/
Manufacturer
Biomet, Inc.
56 E Bell Dr
Warsaw, Indiana 46582
Consumer Instructions Contact the recalling firm for information
Manufacturer Reason
for Recall
The retaining ring may fall out of the instrument during surgery.
FDA Determined
Cause 2
OTHER/UNDETERMINED: Under Investigation by the firm
Action Distributors and consignees were notified by an Urgent Medical Device Recall Notice dated 5/19/09. Distributors and consignees were instructed to locate and remove the devices from circulation, carefully follow the instructions on the "FAX Back Response Form," and fax a copy of the Response Form to 574-372-1683 prior to return of the product. If the product has been further distributed, consignees must notify hospital personnel responsible for receiving recall notices of the action, via the enclosed "Dear Biomet Customer" notice. Consignees are responsible for the location and return of products to the firm. The letter stated that the instruments would be reworked and returned.
Quantity in Commerce 387 of all products
Distribution Worldwide Distribution -- USA, Australia, Belgium, Canada, Costa Rica, Finland, France, Germany, Mexico, New Zealand, Poland, South Wales, and Spain.
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.
510(K) Database 510(K)s with Product Code = KRO and Original Applicant = BIOMET, INC.
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