Device recall
Z-2202-2015: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHITECT…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-2202-2015 |
|---|---|
| Recall event | 71473 |
| Product | ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHITECT cSystem is intended for In Vitro diagnostic use only. It is designed to perform automated: chemistry tests, utilizing photometry and potentiometric technology. |
| Product code | JJE |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 9, 2016 |
| 510(k) numbers | K980367 |
| FEI number | 1415939 |
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