GREENSTONE BRAND fluconazole for Oral Suspension — Class II drug recall D-1356-2014
Terminated recall by Pfizer Inc., reported 2014-06-11, distributed nationwide. Defective Container: Tamper evident ring failures discovered on some bottles.
| Recall number | D-1356-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pfizer Inc., New York, NY, United States |
| Recall initiated | 2014-01-29 |
| Classified | 2014-05-30 |
| Reported by FDA | 2014-06-11 |
| Terminated | 2017-03-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | IT, KR |
| Quantity | 4,155 bottles |
| Reason classes | packaging |
| NDC | 59762-5015, 59762-5015-01, 59762-5016, 59762-5016-01, 59762-5017, 59762-5017-01, 59762-5018, 59762-5018-01, 59762-5029, 59762-5029-01, 59762-5030, 59762-5030-01 |
| Lot numbers | 01/15, A358502 |
Product
GREENSTONE BRAND fluconazole for Oral Suspension, ORANGE FLAVORED, 40 mg/mL, when reconstituted, Rx only, Distributed by Greenstone LLC Peapack, NJ 07977. MADE IN INDIA. NDC 59762-5030-1
Reason for recall
Defective Container: Tamper evident ring failures discovered on some bottles.
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-1356-2014. 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.