Drug recall
Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses…
FDA recall event 73213 · Class III · Volk Optical Inc
Key facts
| Event ID | 73213 |
|---|---|
| Recall numbers | Z-1177-2016 |
| Recalling firm | Volk Optical Inc |
| Product type | Devices |
| Products | Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses for eye examinations (including the anterior chamber, trabecular meshwork, central retina… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The firm discovered that the incorrect lot number was engraved on the product. |
| Initiation date | Feb 2, 2016 |
| Report date | Mar 23, 2016 |
| Termination date | Apr 26, 2017 |
| City | Mentor |
| State | OH |
| Country | United States |
| FEI number | 1000122772 |
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: