Device recall
Z-2463-2021: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites…
FDA device recall · Class II · CAREFUSION
Key facts
| Recall number (Z-number) | Z-2463-2021 |
|---|---|
| Recall event | 88203 |
| Product | BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites, REF: CM42500E-07; BD Gravity IV Set 3-port Closed Stopock Manifold Back Check Valve 2 Needle-Free Y-sites, REF: CS42522E-07; BD GRAVITY 10 DP V/NV CHECK VALVE 3-WAY STOPCOCK 4 Smartsite VALVES & SmartSite EXT SET, REF… |
| Product code | FPA |
| Recalling firm | CAREFUSION |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K931173 |
| FEI number | 3012410077 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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