Device recall
Z-0832-2013: CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood…
FDA device recall · Class II · Carefusion 303 Inc
Key facts
| Recall number (Z-number) | Z-0832-2013 |
|---|---|
| Recall event | 64204 |
| Product | CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer blood and blood products through a needle or catheter inserted into the patient's artery or vein. |
| Product code | FPA |
| Recalling firm | Carefusion 303 Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2013 |
| 510(k) numbers | K882302 |
| FEI number | 3003879246 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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