Device recall
Z-0119-2019: McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product…
FDA device recall · Class II · Cypress Medical Products LLC
Key facts
| Recall number (Z-number) | Z-0119-2019 |
|---|---|
| Recall event | 81113 |
| Product | McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product Usage: Indication of Use: Injection of U-100 insulin only. |
| Product code | FMF |
| Recalling firm | Cypress Medical Products LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 28, 2024 |
| 510(k) numbers | K993017 |
| FEI number | 1451040 |
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