Exact FDA event identifier

Event 74011

1 recalled-product record grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: April 22, 2016
Product types: Drug
Classifications: Class III
Statuses: Terminated
Recalling firm wording: A-S Medication Solutions LLC.

Dossier provenance

Source snapshots represented here

openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-0839-2016

Recall number: D-0839-2016
Initiated: April 22, 2016
Classification: Class III
Status: Terminated
Recalling firm: A-S Medication Solutions LLC.
Quantity: 2730 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

label was incorrect

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Not elsewhere classified - count on the label was incorrect.

Code information

Lot # 6050129, Exp 05/31/17

Distribution pattern

Virginia