Device recall
Z-2297-2021: DELTAVEN FASTFLASH, Safety I.V. Catheter in Pur with closed system: a) REF…
FDA device recall · Class II · Delta Med SpA
Key facts
| Recall number (Z-number) | Z-2297-2021 |
|---|---|
| Recall event | 88234 |
| Product | DELTAVEN FASTFLASH, Safety I.V. Catheter in Pur with closed system: a) REF 3814773 b) REF 3835773 c) REF 3825773 d) REF 3837773 e) REF 3846773 f) REF 3831473 g) REF 3842473 h) REF 3821473 i) REF 3832473 j) REF 3833473 k) REF 3821573 l) REF 3831573 m) REF 3833573 n) REF 3824773 o) REF 3804773 p) REF… |
| 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