Device recall
Z-1636-2016: ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for…
FDA device recall · Class I · Hummingbird Med
Key facts
| Recall number (Z-number) | Z-1636-2016 |
|---|---|
| Recall event | 72350 |
| Product | ABG-HM-1 Hummi Micro Draw Blood Transfer Device Product Usage: It is used for blood transfer and collection from Peripheral Arterial Line Catheters. |
| Product code | KST |
| Recalling firm | Hummingbird Med |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 26, 2017 |
| FEI number | 3009382876 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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