Device recall
Z-1222-2010: Publix Sterile Preserved Saline Solution 12oz, Product SKU#041415-003767. This…
FDA device recall · Class II · K C Pharmaceuticals Inc
Key facts
| Recall number (Z-number) | Z-1222-2010 |
|---|---|
| Recall event | 54656 |
| Product | Publix Sterile Preserved Saline Solution 12oz, Product SKU#041415-003767. This product is supplied in 12 fl. oz. (355 mL) bottles for use in rinsing of soft (hydrophilic) contact lenses after heat (thermal) disinfection and rinsing of contact lenses following chemical disinfection. |
| Product code | LYL |
| Recalling firm | K C Pharmaceuticals Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2011 |
| PMA numbers | P930005 |
| FEI number | 2026940 |
At a glance
- None 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