Device recall
Z-0651-2017: PeroxiClear Peroxide Solution, (3oz. and 12 oz., 12 oz. Twin Pack, 2x12 oz. Twin…
FDA device recall · Class II · Bausch & Lomb Inc Irb
Key facts
| Recall number (Z-number) | Z-0651-2017 |
|---|---|
| Recall event | 75324 |
| Product | PeroxiClear Peroxide Solution, (3oz. and 12 oz., 12 oz. Twin Pack, 2x12 oz. Twin Pack for Target stores, 12 oz. for Walmart Vision Center and 3 oz. Starter Kit US), Manufactured by Bausch + Lomb, Rochester, NY 14609. PeroxiClear 3% Hydrogen Peroxide Cleaning & Disinfecting Solution is indicated for… |
| Product code | LPN |
| Recalling firm | Bausch & Lomb Inc Irb |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2018 |
| 510(k) numbers | K132216 |
| FEI number | 1317628 |
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