Device recall
Z-0890-2013: Atrapro Antipruritic Hydrogel, 1.5 oz gel tube, 4 Net wt/ 1.5 oz.. RX only…
FDA device recall · Class II · Oculus Innovative Sciences Inc
Key facts
| Recall number (Z-number) | Z-0890-2013 |
|---|---|
| Recall event | 64316 |
| Product | Atrapro Antipruritic Hydrogel, 1.5 oz gel tube, 4 Net wt/ 1.5 oz.. RX only, Professional Sample, Not for Sale. Pre-printed tube: MS31071, Shelf carton: PL51091-08 Atrapro Antipruritic HydroGel is indicated to manage and relieve the burning, itching and pain experienced with various types of… |
| Product code | FRO |
| Recalling firm | Oculus Innovative Sciences Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 25, 2013 |
| 510(k) numbers | K012945 |
| FEI number | 3004554409 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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