Device recall
Z-1092-2007: COMPLETE MOISTUREPLUS MULTIPURPOSE SOLUTION, Formula 9451X; (A) Fourteen US…
FDA device recall · Class I · Advanced Medical Optics, Inc.
Key facts
| Recall number (Z-number) | Z-1092-2007 |
|---|---|
| Recall event | 38019 |
| Product | COMPLETE MOISTUREPLUS MULTIPURPOSE SOLUTION, Formula 9451X; (A) Fourteen US Product Numbers distributed under the COMPLETE MOISTUREPLUS MULTIPURPOSE SOLUTION brand include: 90104 (MoisturePLUS, 12 oz ), 90105 (MoisturePLUS, 2 X 12 oz), 90106 (Complete MoisturePLUS Lens Comfort Pack), 90168 (Complete… |
| Product code | LPN |
| Recalling firm | Advanced Medical Optics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 10, 2012 |
| 510(k) numbers | K023226 |
| FEI number | 3003843509 |
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