Device recall
Z-2467-2021: BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD…
FDA device recall · Class II · CAREFUSION
Key facts
| Recall number (Z-number) | Z-2467-2021 |
|---|---|
| Recall event | 88203 |
| Product | BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartSite J-LOOP Extension Set One Needle Free Valve, REF: 20021E7D; BD SmartSite Extension Set One Needle Free Valve Slip Luer, REF: 20037E7D; BD SmartSite Extension Set 3 Needle Free Valves, REF: 20038E7D; BD SmartSite… |
| Product code | FPA |
| Recalling firm | CAREFUSION |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K960280 |
| 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