CIPROFLOXACIN OPHTH SOLUTION — Class II drug recall D-0364-2025
Ongoing recall by Direct Rx, reported 2025-04-23, distributed in AL, CA, FL, GA, ID. Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the no
| Recall number | D-0364-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Direct Rx, Dawsonville, GA, United States |
| Recall initiated | 2025-01-31 |
| Classified | 2025-04-15 |
| Reported by FDA | 2025-04-23 |
| Distributed | AL, CA, FL, GA, ID |
| Quantity | 477 bottles |
| Reason classes | packaging |
| NDC | 61919-0795-05 |
| Lot numbers | 11SE2402, 14NO2406, 29OC2420, 30SE2412 |
| Expiration dates | 2025-11-30, 2025-12-31 |
Product
CIPROFLOXACIN OPHTH SOLUTION, 0.3% 5mL bottle, Rx Only, Generic for CILOXAN, Packaged and Distributed by: DIRECT Rx, NDC 61919-795-05.
Reason for recall
Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
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-0364-2025. 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.