Device recall
Z-1348-2013: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes…
FDA device recall · Class II · Progressive Medical Inc
Key facts
| Recall number (Z-number) | Z-1348-2013 |
|---|---|
| Recall event | 64931 |
| Product | Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated Needle 2.75" (6.99cm) Length, Product number P0013M, Rx Only. Sterilized by Radiation. Manufactured for Progressive Medical, Inc., St. Louis, MO 63128. Electrodes used in… |
| Product code | GEI |
| Recalling firm | Progressive Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2014 |
| FEI number | 3000236238 |
At a glance
- None Linked 510(k)s
- 10–99 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