Device recall
Z-2911-2020: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is…
FDA device recall · Class II · C.A. Greiner & Sohne Gesellschaftmbh
Key facts
| Recall number (Z-number) | Z-2911-2020 |
|---|---|
| Recall event | 86128 |
| Product | Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports. |
| Product code | FMI |
| Recalling firm | C.A. Greiner & Sohne Gesellschaftmbh |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 6368 |
At a glance
- None 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