Exact FDA event identifier

Event 78952

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

Event summary

Timeline bucket: January 17, 2018
Product types: Drug
Classifications: Class I
Statuses: Terminated
Recalling firm wording: Magno Humphries Laboratories, Inc

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

Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.

D-0342-2018

Recall number: D-0342-2018
Initiated: January 17, 2018
Classification: Class I
Status: Terminated
Recalling firm: Magno Humphries Laboratories, Inc
Quantity: 2,400 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

Labeling: Label Mix-Up

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.

Code information

Lot # 352300, Exp 01/19

Distribution pattern

Nationwide in the USA