Device recall
Z-1624-2016: Hamilton G5 with software version between v2.41, v2.42, v2.50. Catalog number…
FDA device recall · Class II · Hamilton Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1624-2016 |
|---|---|
| Recall event | 73816 |
| Product | Hamilton G5 with software version between v2.41, v2.42, v2.50. Catalog number: 1590001 and 1590002. Anesthesiology: Hamilton G5 ventilator is designed for intensive care ventilation of adult and pediatric patients, and optionally infants and neonatal patients. The device is intended for use in the… |
| Product code | CBK |
| Recalling firm | Hamilton Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2017 |
| 510(k) numbers | K070513, K103803, K131774 |
| FEI number | 2937708 |
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