Device recall
Z-0488-2014: 1) Nephros SafeShower FH - 15 filters per box; item no. 70-0236 2) Nephros…
FDA device recall · Class I · Nephros Inc
Key facts
| Recall number (Z-number) | Z-0488-2014 |
|---|---|
| Recall event | 66736 |
| Product | 1) Nephros SafeShower FH - 15 filters per box; item no. 70-0236 2) Nephros SafeShower HH -6 filters per box ; item no. 10-0237 Manufactured by : Nephros, Inc. 41 Grand Ave, River Edge, NJ 07661 Assembled at MEDICA 41036 Medolla, Italy The Nephros SafeSpout and SafeShower are intended to filter water… |
| 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