Device recall
Z-0672-2013: Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2%…
FDA device recall · Class I · Bausch and Lomb, Incorporated
Key facts
| Recall number (Z-number) | Z-0672-2013 |
|---|---|
| Recall event | 63698 |
| Product | Bausch and Lomb 27G sterile cannula packed in the Bausch and Lomb Amvisc 1.2% Sodium Hyaluronate ( Model 59051, 59081, 59051L, 59081L) and Amvisc Plus 1.6% Sodium Hyaluronate (Model 60081, 60051, 60051L, 60081L) ophthalmic viscosurgical device. The 27G disposable cannula is attached to the syringe… |
| Product code | HMX |
| Recalling firm | Bausch and Lomb, Incorporated |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 4, 2013 |
| FEI number | 3004343135 |
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