Device recall
Z-2522-2025: Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer…
FDA device recall · Class II · ICU Medical Inc.
Key facts
| Recall number (Z-number) | Z-2522-2025 |
|---|---|
| Recall event | 97317 |
| Product | Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included. 50mL, Product Code 21-7001-24 |
| Product code | FPA |
| Recalling firm | ICU Medical Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K040636 |
| FEI number | 3012307300 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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