Class III — Volk Optical Inc
| Recalling firm | VOLK OPTICAL INC. |
|---|---|
| Registered facility | VOLK OPTICAL INC. (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | The firm discovered that the incorrect lot number was engraved on the product. |
| Product | 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, and peripheral retina) and use in the therapy of intraocular abnormalities |
| Quantity | 9 lens |
| Distribution | Worldwide Distribution - US (Virginia only) Internationally to Canada, France & Indonesia. |
| Initiated | 2016-02-02 |
| Classified | 2016-03-15 |
| Terminated | 2017-04-26 |
| Recall number | Z-1177-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Volk Optical Inc (Z-1177-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73213/
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