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Synvasive Technology Inc recalls The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, Syste
Recalled April 24, 2013 · FDA recall Z-1127-2013 · Synvasive Technology
Hazard
Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade. · FDA Class II
Units
100 kits
Sold at
USA Nationwide Distributor including the state of IN
Description
Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
Product
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.
Manufacturer(s)
Synvasive Technology Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →