Device recall
Z-0028-05: SOLO-care Plus with Aqualube, Multi-purpose solution*** AquaSoft (Private…
FDA device recall · Class II · Ciba Vision Corporation
Key facts
| Recall number (Z-number) | Z-0028-05 |
|---|---|
| Recall event | 30159 |
| Product | SOLO-care Plus with Aqualube, Multi-purpose solution*** AquaSoft (Private label), Multi-purpose solution***Sterile***For soft lenses, CIBA Vision Corporation, Made in Canada, Assembled in Canada, Manufactured for: CIBA Vision Corporation, Duluth, GA 30097 USA. The product is distributed in units of… |
| Product code | LPN |
| Recalling firm | Ciba Vision Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2005 |
| 510(k) numbers | K031522 |
| FEI number | 1053053 |
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