Device recall
Z-0449-2012: Puracyn OTC; Wound & Skin Care Solution with Preservatives; Sold in 8 fl oz…
FDA device recall · Class II · Oculus Innovative Sciences Inc
Key facts
| Recall number (Z-number) | Z-0449-2012 |
|---|---|
| Recall event | 60387 |
| Product | Puracyn OTC; Wound & Skin Care Solution with Preservatives; Sold in 8 fl oz (trigger spray and finder pump) and 16 fl oz pump with insert. Kills 99.99% of Staph, MRSA, Strep and other Infectious Germs in 30 seconds in solution. Does not contain Antibiotics, Steroids or Alcohol. -Cleans infected… |
| Product code | FRO |
| Recalling firm | Oculus Innovative Sciences Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 7, 2012 |
| 510(k) numbers | K090206 |
| 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