Dexamethasone Sodium Phosphate PF 24 mg/mL Injection — Class II drug recall D-1569-2019
Terminated recall by Wise Pharmacy, reported 2019-08-07, distributed in CO, TX, WY. Lack of Processing Controls
| Recall number | D-1569-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wise Pharmacy, Littleton, CO, United States |
| Recall initiated | 2019-07-22 |
| Classified | 2019-07-31 |
| Reported by FDA | 2019-08-07 |
| Terminated | 2020-02-03 |
| Distributed | CO, TX, WY |
| Quantity | 27 vials |
| Lot numbers | 5506N, 7180N |
| Expiration dates | 2019-09-21, 2019-12-29 |
Product
Dexamethasone Sodium Phosphate PF 24 mg/mL Injection, Refrigerate, Single Use Vial, 1 mL vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
Reason for recall
Lack of Processing Controls
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-1569-2019. 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.