Contamac — Class II medical device recall Z-1956-2025
Ongoing recall by Contamac Solutions, Inc., reported 2025-06-18, distributed nationwide. Contact lens insertion solution may lack sterility.
| Recall number | Z-1956-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Contamac Solutions, Inc., Grand Junction, CO, United States |
| Recall initiated | 2025-05-15 |
| Classified | 2025-06-11 |
| Reported by FDA | 2025-06-18 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00850012123002 |
Product
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Reason for recall
Contact lens insertion solution may lack sterility.
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-1956-2025. 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.