Howmedica Osteonics Corp.: Medical Device Recall in 2021 - (Recall #: Z-0314-2022)

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:

28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122

Product Classification:

Class II

Date Initiated: October 15, 2021

Date Posted: December 8, 2021

Recall Number: Z-0314-2022

Event ID: 88964

Reason for Recall:

There is a potential for the outer white Tyvek lid to debond from the sealed package.

Status: Ongoing

Product Quantity:

Code Information:

UDI number - (01) 07613327013016(17)261013(10); lot numbers - 86604305, 86604306

Distribution Pattern:

Puerto Rico

Voluntary or Mandated:

Voluntary: Firm initiated