Device recall
Z-1557-2011: AquaRefresh, Multi-Purpose Solution, 2 fl.oz/60mL, Made in the Netherlands…
FDA device recall · Class III · Marietta Vision
Key facts
| Recall number (Z-number) | Z-1557-2011 |
|---|---|
| Recall event | 58008 |
| Product | AquaRefresh, Multi-Purpose Solution, 2 fl.oz/60mL, Made in the Netherlands, Distributed by Marietta Vision, 397 N. Sessions Street, Marietta, GA 30060. Contact lens solutions used to clean, rinse, disinfect, rewet and store all soft contact lenses |
| Product code | LPN |
| Recalling firm | Marietta Vision |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 3, 2011 |
| FEI number | 1000140384 |
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