Nutrifill Scleral — Class II medical device recall Z-0030-2022
Terminated recall by Contamac Solutions, Inc., reported 2021-10-13, distributed nationwide. Contact lens solution may contain foreign material
| Recall number | Z-0030-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Contamac Solutions, Inc., Grand Junction, CO, United States |
| Recall initiated | 2021-07-27 |
| Classified | 2021-10-05 |
| Reported by FDA | 2021-10-13 |
| Terminated | 2023-06-07 |
| Distributed | Nationwide (US) |
| Quantity | 104,335 vials |
| Reason classes | foreign material |
| UPC / GTIN / UDI-DI | 00850012123002 |
Product
Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002
Reason for recall
Contact lens solution may contain foreign material
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0030-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.