Synvasive Technology Inc: Medical Device Recall in 2013 - (Recall #: Z-1127-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product 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.

Product Classification:

Class II

Date Initiated: March 14, 2013

Date Posted: April 24, 2013

Recall Number: Z-1127-2013

Event ID: 64646

Reason for Recall:

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

Status: Terminated

Product Quantity: 100 kits

Code Information:

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

Distribution Pattern:

USA Nationwide Distributor including the state of IN

Voluntary or Mandated:

Voluntary: Firm initiated