Device recall
Z-2672-2026: GORE TAG Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers…
FDA device recall · Class II · W L Gore & Associates, Inc.
Key facts
| Recall number (Z-number) | Z-2672-2026 |
|---|---|
| Recall event | 99140 |
| Product | GORE TAG Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes Puerto Rico) and Canada: TSB080806A, TSB081006A, TSB081206A, TSB081506A, TSB081706A, TSB121506A, TSB121706A, TSB122006A EMEA Countries, Australia, New Zealand: TSB080806E, TSB081006E… |
| Product code | MIH |
| Recalling firm | W L Gore & Associates, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P210032 |
| FEI number | 2017233 |
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