Device recall
Z-1422-2018: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP, 16G X 100MM DISP, 17G X 100MM, 16G X…
FDA device recall · Class II · Carefusion 2200 Inc
Key facts
| Recall number (Z-number) | Z-1422-2018 |
|---|---|
| Recall event | 76620 |
| Product | JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP, 16G X 100MM DISP, 17G X 100MM, 16G X 70MM DISP]; STERILE; |
| Product code | FSH |
| Recalling firm | Carefusion 2200 Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 9, 2019 |
| 510(k) numbers | K813338 |
| FEI number | 3008002452 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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