FDA Device recall Z-1849-2019
Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
- FDA Device
- Class II
- terminated
- Published 2019-06-26
On 2019-06-26 the FDA classified a Class II recall of Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1 by Stryker, citing the seal integrity of the sterile bag containing the kits may be compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1849-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-30 |
| Published | 2019-06-26 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Stryker |
| Distribution | US |
Product
Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
Reason
The seal integrity of the sterile bag containing the kits may be compromised.
Identifiers
| code_info | Lot #s 01404, 01478 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1849-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.