FDA Drug recall D-0839-2016
Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, 15-count plastic bottle, Rx only, Mfr: Aurolife Pharma LLC, Dayton NJ, Packaged Ex…
- FDA Drug
- Class III
- terminated
- Published 2016-05-11
On 2016-05-11 the FDA classified a Class III recall of Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, 15-count plastic bottle, Rx only, Mfr: Aurolife Pharma LLC, Dayton NJ, Packaged Ex… by A S Medication Solutions, citing labeling: Not elsewhere classified - count on the label was incorrect.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0839-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-04-22 |
| Published | 2016-05-11 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | A S Medication Solutions |
| Distribution | VA |
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
Labeling: Not elsewhere classified - count on the label was incorrect.
Identifiers
| code_info | Lot # 6050129, Exp 05/31/17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0839-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.