FDA Drug recall D-0483-2020
FreshKote Lubricant Eye Drops, Product Size: 15 mL, NDC 15821-101-15
- FDA Drug
- Class II
- completed
- Published 2019-11-27
On 2019-11-27 the FDA classified a Class II recall of FreshKote Lubricant Eye Drops, Product Size: 15 mL, NDC 15821-101-15 by Altaire Pharmaceuticals, citing lack of Assurance of Sterility.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0483-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2019-07-02 |
| Published | 2019-11-27 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Altaire Pharmaceuticals |
| Distribution | US |
Product
FreshKote Lubricant Eye Drops, Product Size: 15 mL, NDC 15821-101-15
Reason
Lack of Assurance of Sterility
Identifiers
| code_info | Lot #: 18095, Exp 4/20 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0483-2020%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.