Drug recall
Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior…
FDA recall event 67755 · Class II · Alcon LenSx, Inc.
Key facts
| Event ID | 67755 |
|---|---|
| Recall numbers | Z-1445-2014 |
| Recalling firm | Alcon LenSx, Inc. |
| Product type | Devices |
| Products | Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofragmentation. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Alcon LenSx received reports of unexpected downward motion of the gantry. |
| Initiation date | Mar 14, 2014 |
| Report date | Apr 16, 2014 |
| Termination date | Oct 16, 2014 |
| City | Aliso Viejo |
| State | CA |
| Country | United States |
| FEI number | 3008772169 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: