Device recall
Z-0565-2015: ASEPT Peritoneal Drainage System, Ref No. P09080002 Product Usage: The pfm…
FDA device recall · Class II · Pfm Medical Inc
Key facts
| Recall number (Z-number) | Z-0565-2015 |
|---|---|
| Recall event | 69666 |
| Product | ASEPT Peritoneal Drainage System, Ref No. P09080002 Product Usage: The pfm medical ASEPT Peritoneal Drainage System is a tunneled, indwelling catheter used to drain accumulated fluid from the abdomen. |
| Product code | LJS |
| Recalling firm | Pfm Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 23, 2015 |
| 510(k) numbers | K083873 |
| FEI number | 3013666218 |
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