Acetaminophen & Codeine Phosphate Tablets — Class III drug recall D-0839-2016
Terminated recall by A-S Medication Solutions LLC., reported 2016-05-11, distributed in VA. Labeling: Not elsewhere classified - count on the label was incorrect.
| Recall number | D-0839-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | A-S Medication Solutions LLC., Libertyville, IL, United States |
| Recall initiated | 2016-04-22 |
| Classified | 2016-05-05 |
| Reported by FDA | 2016-05-11 |
| Terminated | 2016-10-20 |
| Distributed | VA |
| Quantity | 2,730 bottles |
| Reason classes | labeling |
| NDC | 54569-8305-00 |
| Lot numbers | 6050129 |
| Expiration dates | 2017-05-31 |
Product
Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, 15-count plastic bottle, Rx only, Mfr: Aurolife Pharma LLC, Dayton NJ, Packaged Exclusively by: A-S Medication Solutions LLC, Libertyville, ILL 60048, NDC 54569-8305-0
Reason for recall
Labeling: Not elsewhere classified - count on the label was incorrect.
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-0839-2016. 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.