Device recall
Z-0689-2020: Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0689-2020 |
|---|---|
| Recall event | 84054 |
| Product | Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit, Product Code 9001P-VC-005 - Product Usage: The Arrow EZ-IO Intraosseous Vascular Access System provides intraosseous access in the proximal humerus, proximal tibia, and distal tibia of adult and pediatric patients, and the… |
| Product code | FMI |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K141117 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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