Howmedica Osteonics Corp.: Medical Device Recall in 2021 - (Recall #: Z-2329-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700

Product Classification:

Class II

Date Initiated: July 1, 2021

Date Posted: August 25, 2021

Recall Number: Z-2329-2021

Event ID: 88422

Reason for Recall:

The internal profile of the Triathlon Prim (Baseplate) is potentially oversized; there may be a witness mark (taper) at the bottom of the internal profile of the baseplate, which prevents the insert from locking on the baseplate.

Status: Terminated

Product Quantity: 14 US; 2 OUS

Code Information:

Lot JHS2H

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states AR, CO, MN, MS, NJ, OK, PA, TX and the countries of China and Italy.

Voluntary or Mandated:

Voluntary: Firm initiated