Device recall
Z-1208-03: Software Versions V1.2R,or earlier for the Harvard 2, Dual Infusion Pump (P/N…
FDA device recall · Class II · Harvard Clinical Technology
Key facts
| Recall number (Z-number) | Z-1208-03 |
|---|---|
| Recall event | 26903 |
| Product | Software Versions V1.2R,or earlier for the Harvard 2, Dual Infusion Pump (P/N 2002-001) |
| Product code | FRN |
| Recalling firm | Harvard Clinical Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2012 |
| 510(k) numbers | K952794 |
| FEI number | 1218257 |
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