FDA Device recall Z-1177-2016
Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses for eye examinations (includin…
- FDA Device
- Class III
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class III recall of Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602 for use as diagnostic contact lenses for eye examinations (includin… by Volk Optical, citing the firm discovered that the incorrect lot number was engraved on the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1177-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-02-02 |
| Published | 2016-03-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Volk Optical |
| Distribution | VA |
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
Reason
The firm discovered that the incorrect lot number was engraved on the product.
Identifiers
| upc | 811608013602 |
|---|---|
| code_info | Model #: VG4SNF, Lot: BE05200 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1177-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.