Device recall
Z-0564-04: CordisEndomyocardial Biopsy Forceps 7F 104 cm Standard, Product Number 504300L
FDA device recall · Class III · Cordis Corporation
Key facts
| Recall number (Z-number) | Z-0564-04 |
|---|---|
| Recall event | 27138 |
| Product | CordisEndomyocardial Biopsy Forceps 7F 104 cm Standard, Product Number 504300L |
| Product code | GEN |
| Recalling firm | Cordis Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 7, 2004 |
| FEI number | 1016427 |
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