CLEAR EYES Maximum Itchy Eye Relief — Class II drug recall D-0766-2026
Ongoing recall by Prestige Brands Holdings, reported 2026-08-19, distributed nationwide. Lack of assurance of sterility. The recall is due to potential contamination
| Recall number | D-0766-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Prestige Brands Holdings, Tarrytown, NY, United States |
| Recall initiated | 2026-07-29 |
| Classified | 2026-08-14 |
| Reported by FDA | 2026-08-19 |
| Distributed | Nationwide (US) |
| Quantity | 39,060 |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00678112659203 |
| NDC | 67172-0999-01 |
| Lot numbers | 2552A |
| Expiration dates | 2027-09-30 |
Product
CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3
Reason for recall
Lack of assurance of sterility. The recall is due to potential contamination
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/D-0766-2026. 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.