Device recall
Z-0268-2008: Pilling Center-Action Forceps with Insulated Shafts- Circular Cup Biopsy Jaws…
FDA device recall · Class II · Telefelx Medical
Key facts
| Recall number (Z-number) | Z-0268-2008 |
|---|---|
| Recall event | 45515 |
| Product | Pilling Center-Action Forceps with Insulated Shafts- Circular Cup Biopsy Jaws, Catalog Number: 505045, Non Sterile, Rx Only, (30 CM), Manufactured for: Teleflex Medical, Research Triangle Park, NC 27709 USA |
| Product code | HTD |
| Recalling firm | Telefelx Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 31, 2009 |
| FEI number | 3005747797 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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