Device recall
Z-2584-2010: WECK IMA/ENT Blade Electrode (1.9 cm), REF 809335, Rx Only Sterile, Teleflex…
FDA device recall · Class II · Telefelx Medical
Key facts
| Recall number (Z-number) | Z-2584-2010 |
|---|---|
| Recall event | 56379 |
| Product | WECK IMA/ENT Blade Electrode (1.9 cm), REF 809335, Rx Only Sterile, Teleflex Medical, RTP, NC The blade electrode is used in a wide variety of surgical procedures. The most common uses for electrodes with extended insulation is in cardiac bypass surgery (used in the take-down of the internal mammary… |
| Product code | GEI |
| Recalling firm | Telefelx Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 21, 2011 |
| FEI number | 3005747797 |
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