Dextroamphetamine Saccharate — Class II drug recall D-1485-2016
Terminated recall by Amerisource Health Services, reported 2016-09-14, distributed nationwide. Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
| Recall number | D-1485-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Amerisource Health Services, Columbus, OH, United States |
| Recall initiated | 2016-08-24 |
| Classified | 2016-09-02 |
| Reported by FDA | 2016-09-14 |
| Terminated | 2017-12-18 |
| Distributed | Nationwide (US) |
| Quantity | 156 cartons |
| NDC | 60687-0154-25, 60687-0154-95 |
| Lot numbers | 162278 |
| Expiration dates | 2017-10-31 |
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 60687-154-25; Blister NDC 60687-154-95
Reason for recall
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
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-1485-2016. 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.