Device recall
Z-2705-2016: Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide…
FDA device recall · Class II · Medical Vision Ab
Key facts
| Recall number (Z-number) | Z-2705-2016 |
|---|---|
| Recall event | 74190 |
| Product | Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures. |
| Product code | HRX |
| Recalling firm | Medical Vision Ab |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2017 |
| 510(k) numbers | K093409 |
| FEI number | 3003647329 |
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