FDA Enforcement Class II Terminated

The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage: For use with Stryker System 5, System 4, System 2000 and EDH. A set of three surgical saw blades is used to resect damaged cartilage and/or bone in an orthopedic reconstructive procedure such as a partial knee replacement. The set contains both oscillating blades for tissue resection along a small arc in a left/right or up/down direction, and reciprocating blades for resection back and forth in a single plane.

Recall: Z-1127-2013 · Reported April 24, 2013

Enforcement

Recall Number
Z-1127-2013
Event ID
64646
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Synvasive Technology Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
April 24, 2013
Initiation Date
March 14, 2013
Classification Date
April 16, 2013
Termination Date
January 13, 2014
Address
4925 Robert J Mathews Pkwy, N/A, El Dorado Hills, CA, 95762-5701, United States

Description

The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage: For use with Stryker System 5, System 4, System 2000 and EDH. A set of three surgical saw blades is used to resect damaged cartilage and/or bone in an orthopedic reconstructive procedure such as a partial knee replacement. The set contains both oscillating blades for tissue resection along a small arc in a left/right or up/down direction, and reciprocating blades for resection back and forth in a single plane.

Reason

Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.

Code Info

Biomet Product code: 506076, Lot 829182. Synvasive Part Number: 11-3629.

Distribution

USA Nationwide Distributor including the state of IN

Quantity

100 kits