FDA Drug recall D-0523-2016
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
- FDA Drug
- Class III
- terminated
- Published 2015-12-30
On 2015-12-30 the FDA classified a Class III recall of 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 by Oasis Medical, citing failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0523-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-10-19 |
| Published | 2015-12-30 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Oasis Medical |
| Distribution | US |
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
Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Identifiers
| code_info | Lot #: V1014M, Exp 10/2016; V1214B, Exp 12/2016; V0415H, Exp 4/2017. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0523-2016%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.