Device recall
Z-0514-06: Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006…
FDA device recall · Class II · Hamilton Co
Key facts
| Recall number (Z-number) | Z-0514-06 |
|---|---|
| Recall event | 34324 |
| Product | Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016, 135028, 135029, 936400, 936400BLU. Microlab AT+ and Microlab AT+2, part numbers 142000, 142001, 142001R, 142002, 142003, 142005, 142006, 142006R, 142007, 142008, 142009, 142015, 142017… |
| Product code | JTC |
| Recalling firm | Hamilton Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2008 |
| 510(k) numbers | K871945 |
| FEI number | 2915796 |
At a glance
- 1–9 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