Z-2400-2021 Class II Terminated

Recalled by DePuy Orthopaedics, Inc. — Warsaw, IN

Recall Details

Product Type
Devices
Report Date
September 8, 2021
Initiation Date
August 10, 2021
Termination Date
May 17, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 cs (1/cs)

Product Description

TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420917

Reason for Recall

Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may not be aligned, causing the anatomic landmark locations to potentially result in limb malalignment.

Distribution Pattern

Distribution to US states of CA, CO, FL, IL, IN, NY, MI, MN, TX, and WA, Poland and UK.

Code Information

Lot number/ GTIN: 27958 10603295384878