Device recall
Z-1894-2020: ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis…
FDA device recall · Class III · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-1894-2020 |
|---|---|
| Recall event | 85394 |
| Product | ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients with abnormal insulin secretion including diabetes mellitus. |
| Product code | JJX |
| Recalling firm | Abbott Laboratories |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 1, 2020 |
| FEI number | 1415939 |
At a glance
- None 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