Stryker GmbH: Medical Device Recall in 2019 - (Recall #: Z-1849-2019)

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 Hook/Triangle Blade Kit, Catalogue Number 3056-1

Product Classification:

Class II

Date Initiated: April 30, 2019

Date Posted: June 26, 2019

Recall Number: Z-1849-2019

Event ID: 82894

Reason for Recall:

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

Status: Terminated

Product Quantity: 1600

Code Information:

Lot #s 01404, 01478

Distribution Pattern:

The products were distributed US nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated