Device recall
Z-0606-2011: Beaver-Visitec International (Beaver-Visitec) BD 1% OVD Sodium Hyaluronate, 10…
FDA device recall · Class II · Becton Dickinson and Company
Key facts
| Recall number (Z-number) | Z-0606-2011 |
|---|---|
| Recall event | 57104 |
| Product | Beaver-Visitec International (Beaver-Visitec) BD 1% OVD Sodium Hyaluronate, 10 mg/ml 1.0 mL. Sterile. Rx For Intraocular Use REF 585304 Use as a surgical aid to protect corneal endothelium during cataract extraction procedures, intraocular lens implantation and anterior segment surgery. |
| Product code | LZP |
| Recalling firm | Becton Dickinson and Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2012 |
| PMA numbers | P960011 |
| FEI number | 1211998 |
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