Device recall
Z-0444-2016: Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable…
FDA device recall · Class II · Myco Medical Supplies Inc
Key facts
| Recall number (Z-number) | Z-0444-2016 |
|---|---|
| Recall event | 72616 |
| Product | Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle |
| Product code | FMI |
| Recalling firm | Myco Medical Supplies Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 3, 2017 |
| 510(k) numbers | K945225 |
| FEI number | 1000158634 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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