Device recall
Z-1341-04: ARCHITECT c8000 Processing Module; List Number 01G06-01. Manufactured by Toshiba…
FDA device recall · Class III · Abbott Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-1341-04 |
|---|---|
| Recall event | 29587 |
| Product | ARCHITECT c8000 Processing Module; List Number 01G06-01. Manufactured by Toshiba Corporation, Medical Systems Division, Japan. Distributed by Abbott Laboratories Diagnostic Division, Irving, Texas |
| Product code | CGZ |
| Recalling firm | Abbott Laboratories, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 19, 2004 |
| 510(k) numbers | K980367 |
| FEI number | 1628664 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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