PlainRecalls
FDA Devices Moderate Class II Terminated

Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1

Reported: June 26, 2019 Initiated: April 30, 2019 #Z-1849-2019

Product Description

Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1

Reason for Recall

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

Details

Recalling Firm
Stryker GmbH
Units Affected
1600
Distribution
The products were distributed US nationwide.
Location
Selzach, N/A

Frequently Asked Questions

What product was recalled?
Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1. Recalled by Stryker GmbH. Units affected: 1600.
Why was this product recalled?
The seal integrity of the sterile bag containing the kits may be compromised.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 26, 2019. Severity: Moderate. Recall number: Z-1849-2019.