Device recall
Z-2225-2023: VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro…
FDA device recall · Class III · Ortho-Clinical Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-2225-2023 |
|---|---|
| Recall event | 92485 |
| Product | VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro diagnostic use only. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used for the quantitative measurement of N-terminal pro… |
| Product code | JJX |
| Recalling firm | Ortho-Clinical Diagnostics, Inc. |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 1000136573 |
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