Howmedica Osteonics Corp.: Medical Device Recall in 2020 - (Recall #: Z-0811-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254

Product Classification:

Class II

Date Initiated: November 7, 2019

Date Posted: January 22, 2020

Recall Number: Z-0811-2020

Event ID: 84346

Reason for Recall:

May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire

Status: Terminated

Product Quantity: 20 units

Code Information:

Lot Number: 53778501 UDIs: (01)04546540035806(17)201108(10)53778501

Distribution Pattern:

CA, FL, GA , IA, MA, MI, NC, OH, WI Foreign: Canada, Japan

Voluntary or Mandated:

Voluntary: Firm initiated