FDA Drug recall D-0392-2019
Cyclosporin liquid 2%, Rx, plastic dropper bottle, dry eye
- FDA Drug
- Class II
- terminated
- Published 2019-01-09
On 2019-01-09 the FDA classified a Class II recall of Cyclosporin liquid 2%, Rx, plastic dropper bottle, dry eye by Hiers Enterprises, citing lack of sterility assurance.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0392-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-02 |
| Published | 2019-01-09 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Hiers Enterprises |
| Distribution | OR |
Product
Cyclosporin liquid 2%, Rx, plastic dropper bottle, dry eye
Reason
Lack of sterility assurance.
Identifiers
| code_info | 08172018@7 exp 2/13/19, 09202018@16 exp 3/2/19, 10172018@32 exp 3/2/19. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0392-2019%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.