Device recall
Z-0159-2013: Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm)…
FDA device recall · Class II · Progressive Medical Inc
Key facts
| Recall number (Z-number) | Z-0159-2013 |
|---|---|
| Recall event | 62386 |
| Product | Progressive Medical PMI Endoscopic Dissector with Kittner Tip (5mm x 40cm), Reorder Number: PMILK40, Product Sterile in Unopened/Undamaged pouch, Cotton Tip - X-Ray Detectable, 1 Pc/Pouch, 10 Pouches/Box, 20 boxes/case. Product Usage: The product is used for pushing tissue from the incision or wound… |
| Product code | GDI |
| Recalling firm | Progressive Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2012 |
| FEI number | 3000236238 |
At a glance
- None Linked 510(k)s
- 1–9 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