Device recall
Z-0562-03: Boston Scientific Microvasive Radial Jaw 3 Single-Use Maximum Capacity Biopsy…
FDA device recall · Class III · Symbiosis Corp.
Key facts
| Recall number (Z-number) | Z-0562-03 |
|---|---|
| Recall event | 25510 |
| Product | Boston Scientific Microvasive Radial Jaw 3 Single-Use Maximum Capacity Biopsy Forceps Needle, 240 cm length, 3.3 mm Jaw Outside Diameter. Each device is pakaged in a Tyvek laminate pouch. The pouch assemblies are packaged in a five-pack product box. |
| Recalling firm | Symbiosis Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 15, 2008 |
| FEI number | 1051710 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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