Device recall
Z-2298-2021: DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF…
FDA device recall · Class II · Delta Med SpA
Key facts
| Recall number (Z-number) | Z-2298-2021 |
|---|---|
| Recall event | 88234 |
| Product | DELTAVEN Y, Safety I.V. Catheter in Pur with closed system a) REF 3832072 b) REF 3810072 c) REF 3842072 d) REF 3852072 |
| Product code | FOZ |
| Recalling firm | Delta Med SpA |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K171530 |
| FEI number | 3006846316 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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