Device recall
Z-0983-2017: Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic…
FDA device recall · Class II · Bausch & Lomb, Inc.
Key facts
| Recall number (Z-number) | Z-0983-2017 |
|---|---|
| Recall event | 75915 |
| Product | Algerbrush-II Product Usage: Medical - For surgeons to use in ophthalmic surgical procedures to remove foreign bodies from the eye of the patient |
| Product code | OHW |
| Recalling firm | Bausch & Lomb, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 14, 2017 |
| FEI number | 1000305478 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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