Device recall
Z-1888-2020: Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA…
FDA device recall · Class II · Inpeco S.A.
Key facts
| Recall number (Z-number) | Z-1888-2020 |
|---|---|
| Recall event | 85429 |
| Product | Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf |
| Product code | JJE |
| Recalling firm | Inpeco S.A. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K121012 |
| FEI number | 3010825766 |
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