Diethylpropion — Class II drug recall D-0010-2021
Terminated recall by Calvin Scott & Company, Inc., reported 2020-10-14, distributed in CA, ID, IL, OK, RI. cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.
| Recall number | D-0010-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Calvin Scott & Company, Inc., Albuquerque, NM, United States |
| Recall initiated | 2020-09-16 |
| Classified | 2020-10-02 |
| Reported by FDA | 2020-10-14 |
| Terminated | 2024-04-22 |
| Distributed | CA, ID, IL, OK, RI |
| Reason classes | specification failure |
| NDC | 00527-1477-01 |
| Lot numbers | 1/22, 10/20, 10/21, 4/22, 7/21, 8/21, CS19192, CS19226, CS19263, CS19300, CS19338, CS20034, CS20077, CS20165, CS20241 |
Product
Diethylpropion, 75 mg tablets, Rx only, Distributed by: Calvin Scott & Co. Inc. Albuquerque, NM 87123; MFG. Lannett Company, Philadelphia, PA 19136, NDC 00527-1477-01
Reason for recall
cMGP Deviations: Drug products repackaged into pouches without supporting stability studies.
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-0010-2021. 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.