Device recall
Z-0172-2007: Asahi Rexeed Series Multiple-Use Hollow Fiber Dialyzers; a wet model multiple…
FDA device recall · Class III · Asahi Medical Co., Ltd
Key facts
| Recall number (Z-number) | Z-0172-2007 |
|---|---|
| Recall event | 36430 |
| Product | Asahi Rexeed Series Multiple-Use Hollow Fiber Dialyzers; a wet model multiple use dialyzer consisting of hollow fiber membranes of polysulfone/PVP housed within a plastic casing of styrene copolymer, filled at the factory with fluid to facilitate priming by the user, and sterilized by gamma… |
| Product code | KDI |
| Recalling firm | Asahi Medical Co., Ltd |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 28, 2007 |
| 510(k) numbers | K051187 |
| FEI number | 1000599821 |
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