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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 72240

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

Open FDA event record

Event summary

Timeline bucket
September 22, 2015
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Midway Importing, 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

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

Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets, 20-count tablets in blisters per box, Manufactured in Mexico by: Merck, S.A. de C.V./, Imported & Distributed by Midway Importing, Inc., 1807 Brittmoore Rd, Houston, TX 77043, UPC: 1 88436 00017 4.

D-0013-2016
Recall number
D-0013-2016
Initiated
September 22, 2015
Classification
Class II
Status
Terminated
Recalling firm
Midway Importing, Inc
Quantity
164,332 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Cross Contamination With Other Products: Potential cross-contamination of cephalosporin.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Cross Contamination With Other Products: Potential cross-contamination of cephalosporin.

Code information

Lot Numbers: M51196, M51197, M51198, Exp 01/17

Distribution pattern

Nationwide