Device recall
Z-0536-2015: An external vein stripper is an extravascular device used to remove a section of…
FDA device recall · Class II · Instrumed International, Inc.
Key facts
| Recall number (Z-number) | Z-0536-2015 |
|---|---|
| Recall event | 69471 |
| Product | An external vein stripper is an extravascular device used to remove a section of a vein sold under the Symmetry Surgical, CareFusion, Boss Instruments, Phoenix Instruments, Autobahn Surgical, Echo Instruments, Millennium Surgical, B.B.M. Surgical Instruments, Stealth Surgical, Medline Industries… |
| Product code | MGZ |
| Recalling firm | Instrumed International, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2017 |
| FEI number | 1421101 |
At a glance
- None Linked 510(k)s
- 10–99 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