Device recall
Z-0682-2024: ARCHITECT c4000 Processing Module REF: 02P24-01 02P24-02 02P24-40 01R24-56…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-0682-2024 |
|---|---|
| Recall event | 93355 |
| Product | ARCHITECT c4000 Processing Module REF: 02P24-01 02P24-02 02P24-40 01R24-56 01R25-56 The Abbott ARCHITECT c4000 Processing Module is designed to perform automated chemistry tests, utilizing photometry and potentiometric technology. |
| Product code | JJE |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3016438761 |
At a glance
- None 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