Device recall
Z-2526-2026: Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
FDA device recall · Class II · PFM MEDICAL INC.
Key facts
| Recall number (Z-number) | Z-2526-2026 |
|---|---|
| Recall event | 98942 |
| Product | Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310 |
| Product code | DXE |
| Recalling firm | PFM MEDICAL INC. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K011783 |
| FEI number | 3013666218 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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