Device recall
Z-1940-2015: Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone…
FDA device recall · Class II · Alcon Research, Ltd.
Key facts
| Recall number (Z-number) | Z-1940-2015 |
|---|---|
| Recall event | 71383 |
| Product | Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone Vitreous Probe REF 8065750821; Accurus 25+ 2500 CPM Standalone Vitreous Probe REF 8065751122; Anterior Accurus Probe with Infusion Needle REF 8065803650; Single Use Sterile Probes Rx only. Intended to provide the surgeon… |
| Product code | HQC |
| Recalling firm | Alcon Research, Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2017 |
| 510(k) numbers | K911808 |
| FEI number | 1610287 |
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