Stryker GmbH: Medical Device Recall in 2019 - (Recall #: Z-2416-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.

Product Classification:

Class II

Date Initiated: July 25, 2019

Date Posted: September 4, 2019

Recall Number: Z-2416-2019

Event ID: 83423

Reason for Recall:

The seal integrity of the sterile bag containing the kits may be compromised.

Status: Terminated

Product Quantity: 251

Code Information:

Lot Numbers 01399, 01464, 01477

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated