Device recall
Z-2490-2020: Prodimed Combicath catheters for blind or fibrescope-guided protected distal…
FDA device recall · Class II · Prodimed Plastimed Division
Key facts
| Recall number (Z-number) | Z-2490-2020 |
|---|---|
| Recall event | 85776 |
| Product | Prodimed Combicath catheters for blind or fibrescope-guided protected distal bronchial sampling (PDBS)- COMBICATH PE 90 cm Product Code: 58229 19 |
| Product code | EOQ |
| Recalling firm | Prodimed Plastimed Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 29, 2021 |
| 510(k) numbers | K974642 |
| FEI number | 3003781614 |
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