Device recall
Z-2296-2021: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b)…
FDA device recall · Class II · Delta Med SpA
Key facts
| Recall number (Z-number) | Z-2296-2021 |
|---|---|
| Recall event | 88234 |
| Product | DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed system: a) REF 3832572 b) REF 3842572 c) REF 3821572 d) REF 3833572 e) REF 3831572 f) REF 3810572 g) REF 3852572 |
| Product code | FOZ |
| Recalling firm | Delta Med SpA |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K200373 |
| 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