HPMC Visoelastic Topical — Class III drug recall D-0523-2016
Terminated recall by Oasis Medical, Inc., reported 2015-12-30, distributed nationwide. Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification a
| Recall number | D-0523-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Oasis Medical, Inc., Glendora, CA, United States |
| Recall initiated | 2015-10-19 |
| Classified | 2015-12-22 |
| Reported by FDA | 2015-12-30 |
| Terminated | 2016-03-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, CA, CH, CL, DE, EC, GB, GR, IL, NO, PK, PL, SA, SV, ZA |
| Quantity | 3,358 units |
| Lot numbers | V0415H, V1014M, V1214B |
| Expiration dates | 2016-10, 2016-12, 2017-04 |
Product
HPMC Visoelastic Topical, 8,000 cps, Reference 5200, 1.5 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
Reason for recall
Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
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-0523-2016. 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.