Device recall
Z-0931-2014: Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model…
FDA device recall · Class II · CareFusion 303, Inc.
Key facts
| Recall number (Z-number) | Z-0931-2014 |
|---|---|
| Recall event | 67326 |
| Product | Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230. |
| Product code | FPA |
| Recalling firm | CareFusion 303, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2014 |
| 510(k) numbers | K051499 |
| FEI number | 2016493 |
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