Device recall
Z-2209-2026: Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1)…
FDA device recall · Class II · TANGENT ENDOSCOPY, LLC
Key facts
| Recall number (Z-number) | Z-2209-2026 |
|---|---|
| Recall event | 98654 |
| Product | Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk. |
| Product code | FBN |
| Recalling firm | TANGENT ENDOSCOPY, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K251170 |
| FEI number | 3041659934 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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