Device recall
Z-1373-2013: EZ Breathe Medication Cup. For the delivery of liquid medications for…
FDA device recall · Class I · Nephron Pharmaceuticals Corp.
Key facts
| Recall number (Z-number) | Z-1373-2013 |
|---|---|
| Recall event | 65070 |
| Product | EZ Breathe Medication Cup. For the delivery of liquid medications for respiratory usage. |
| Product code | CCQ |
| Recalling firm | Nephron Pharmaceuticals Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 28, 2016 |
| FEI number | 3010892830 |
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