Device recall
Z-0487-2014: Nephros SafeSpout Manufacturer: Nephros Inc. 41 Grand Avenue, River Edge, NJ…
FDA device recall · Class I · Nephros Inc
Key facts
| Recall number (Z-number) | Z-0487-2014 |
|---|---|
| Recall event | 66736 |
| Product | Nephros SafeSpout Manufacturer: Nephros Inc. 41 Grand Avenue, River Edge, NJ 07661 Assembled at : MEDICA 41036 Medolla, Italy Filters are packaged in a Tyvek pouch and then placed inside a cardboard box. 15 filters per box The Nephros SafeSpout and SafeShower are intended to filter water for washing… |
| Product code | ND |
| Recalling firm | Nephros Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 28, 2017 |
| FEI number | 3003337893 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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