Howmedica Osteonics Corp.: Medical Device Recall in 2018 - (Recall #: Z-0373-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Sterile Knee Instruments Disposable Fluted Headless Pins, DIA 3.2mm LNTH 89mm, REF 7650-2038A - Product Usage: Howmedica Osteonics Corp. (Stryker, Joint Reconstructive Division) Sterile Instrumentation consists of manual surgical instrumentation intended for use during hip, knee, shoulder, elbow or wrist arthroplasty, or trauma surgeries.

Product Classification:

Class II

Date Initiated: September 10, 2018

Date Posted: November 14, 2018

Recall Number: Z-0373-2019

Event ID: 81192

Reason for Recall:

Potential for outer pouch sterile barrier to be compromised

Status: Terminated

Product Quantity: 15 pouches

Code Information:

Lot SC22130X Exp 2023-08-05

Distribution Pattern:

US Nationwide in the states of AL, FL, IL, MI, NJ & OH.

Voluntary or Mandated:

Voluntary: Firm initiated