Device recall
Z-0879-2013: BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge…
FDA device recall · Class II · Baylis Medical Company Inc.
Key facts
| Recall number (Z-number) | Z-0879-2013 |
|---|---|
| Recall event | 64250 |
| Product | BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge 16 Ga, Length: 100mm. The BMC RF Cannula is sealed in a Tyvek pouch (primary packaging) and then placed into a white shelf-box (secondary packaging) with the instructions for use. A predetermined number of white… |
| Product code | GXI |
| Recalling firm | Baylis Medical Company Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 23, 2013 |
| 510(k) numbers | K972846 |
| FEI number | 3000157372 |
At a glance
- 1–9 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