Device recall
Z-1829-2017: Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
FDA device recall · Class III · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1829-2017 |
|---|---|
| Recall event | 76872 |
| Product | Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079. |
| Product code | FMI |
| Recalling firm | Teleflex Medical |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 19, 2024 |
| 510(k) numbers | K091140 |
| 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