Device recall
Z-2249-2021: TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm…
FDA device recall · Class II · Bard Peripheral Vascular Inc
Key facts
| Recall number (Z-number) | Z-2249-2021 |
|---|---|
| Recall event | 88314 |
| Product | TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 15G x 79mm |
| Product code | KNW |
| Recalling firm | Bard Peripheral Vascular Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K930217 |
| FEI number | 2020394 |
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