FDA Drug recall D-0524-2016
HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue G…
- FDA Drug
- Class III
- terminated
- Published 2015-12-30
On 2015-12-30 the FDA classified a Class III recall of HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue G… 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-0524-2016 |
| 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, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 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 #: V0814C, V0814D, Exp 8/2016; V1014A, V1014B, Exp 10/2016; V1214C, Exp 12/2016; V0115A, V0115B, Exp 01/2017; V02…Lot #: V0814C, V0814D, Exp 8/2016; V1014A, V1014B, Exp 10/2016; V1214C, Exp 12/2016; V0115A, V0115B, Exp 01/2017; V0215C, Exp 02/2017; V0315C, V0315D, Exp 03/2017; V0515A, V0515B, Exp 05/2017. |
|---|
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-0524-2016%22
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