Synthes USA HQ, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0409-2014)

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:

Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.

Product Classification:

Class II

Date Initiated: July 30, 2013

Date Posted: December 4, 2013

Recall Number: Z-0409-2014

Event ID: 66418

Reason for Recall:

The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight Condylar Plate is etched with a Curved Condylar Plate part number.

Status: Terminated

Product Quantity: 13

Code Information:

Part No. 02.001.324, lot no. 6900823

Distribution Pattern:

Worldwide Distribution - USA including ID, FL, TN, NY, LA and Internationally to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated