Recall: A-S Meds Acetaminophen/Codeine Labeling Error
A-S Medication Solutions recalls 15-count bottles of Acetaminophen & Codeine Phosphate due to incorrect count on the label.
Recall notice
Labeling: Not elsewhere classified - count on the label was incorrect.
Contact the company
What happened, in plain English
A-S Medication Solutions LLC is recalling one lot of Acetaminophen & Codeine Phosphate Tablets because the number of pills listed on the bottle's label does not match the actual contents. The product is a prescription-only medication manufactured by Aurolife Pharma LLC. No other details regarding the specific nature of the count error or remediation steps are provided in the record. Read more at govinfonow.com/recall/42863-recall-a-s-meds-acetaminophen-codeine-labeling-error.
Source Summary by GovInfoNow · govinfonow.com/recall/42863-recall-a-s-meds-acetaminophen-codeine-labeling-error · Updated October 11, 2026 · FDA enforcement record: FDA #D-0839-2016
Cite this page
“Recall: A-S Meds Acetaminophen/Codeine Labeling Error.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/42863-recall-a-s-meds-acetaminophen-codeine-labeling-error. Based on FDA recall #D-0839-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0839-2016%22&limit=1).
Why it’s dangerous
The hazard is a labeling discrepancy where the count on the label is incorrect. The record does not specify if the bottle contains fewer or more pills than stated, nor does it describe any resulting health risks or injuries.
Who’s affected
Patients in Virginia who purchased the recalled prescription bottles between the manufacturing date and April 22, 2016, may be affected. Individuals holding this specific lot number should verify their medication against the recall details.
How to tell if you have this one
Check for Acetaminophen & Codeine Phosphate Tablets, 300 mg/30 mg, in a 15-count plastic bottle. Look for NDC 54569-8305-0 and Lot # 6050129 with an expiration date of 05/31/17. The product was manufactured by Aurolife Pharma LLC in Dayton, NJ, and packaged exclusively by A-S Medication Solutions LLC in Libertyville, IL.
- Brand
A-S Medication Solutions- Category
Drug
Where it went and when
Where it was distributed
Distributed in Virginia.
FDA distribution: “Virginia” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Virginia.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Where was this medication distributed?
The distribution pattern listed for this recall is Virginia.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0839-2016 (April 22, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0839-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.