FDA Enforcement Class II Terminated

Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard Complete Knee System. 1. Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. 2. Correction of varus, valgus, or posttraumatic deformity. 3. Correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

Recall: Z-2068-2017 · Reported May 17, 2017

Enforcement

Recall Number
Z-2068-2017
Event ID
77094
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Zimmer Biomet, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
May 17, 2017
Initiation Date
March 22, 2017
Classification Date
May 10, 2017
Termination Date
October 3, 2017
Address
56 E Bell Dr, N/A, Warsaw, IN, 46582-6989, United States

Description

Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard Complete Knee System. 1. Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved. 2. Correction of varus, valgus, or posttraumatic deformity. 3. Correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure.

Reason

pegs shearing post-operatively

Code Info

All lots of Model #'s: 141355 141356 141357 141358

Distribution

US Nationwide.distribution and Canada.

Quantity

8154