Device recall
Z-0776-2017: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F…
FDA device recall · Class III · Angiodynamics, Inc.
Key facts
| Recall number (Z-number) | Z-0776-2017 |
|---|---|
| Recall event | 75420 |
| Product | ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T NON-ECHO S PG, Item Number H787065970655, Catalog No.REF 06597065, 2) 4 F Stiffened Micro-Introducer Kit, STF 4F M.I. KIT 45CM NT/T NON-ECHO S PG, Item Number H787065970695, Catalog… |
| Product code | DYB |
| Recalling firm | Angiodynamics, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 18, 2018 |
| 510(k) numbers | K051655 |
| FEI number | 1319211 |
At a glance
- 1–9 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