Device recall
Z-2295-2021: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) REF 3836272 b) REF…
FDA device recall · Class II · Delta Med SpA
Key facts
| Recall number (Z-number) | Z-2295-2021 |
|---|---|
| Recall event | 88234 |
| Product | DELTAVEN Safety I.V. Catheter in Pur with closed system: a) REF 3836272 b) REF 3814272 c) REF 3845272 d) REF 3856272 |
| 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