Device recall
Z-0043-2026: Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part…
FDA device recall · Class I · Cook Medical Incorporated
Key facts
| Recall number (Z-number) | Z-0043-2026 |
|---|---|
| Recall event | 97615 |
| Product | Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167 ZTA2-P-40-167-W ZTA2-P-40-217-W ZTA2-P-42-121 ZTA2-P-42-121-W ZTA2-P-42-173 ZTA2-P-42-173-W ZTA2-P-42-225 ZTA2-P-42-225-W ZTA2-P-44-125 ZTA2-P-44-125-W ZTA2-P-44-179 ZTA2-P-44-179-W… |
| Product code | MIH |
| Recalling firm | Cook Medical Incorporated |
| Recall class | Class I |
| Status | Open, Classified |
| PMA numbers | P140016 |
| FEI number | 3005580113 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database