Sedalmex — Class II drug recall D-0013-2016
Terminated recall by Midway Importing, Inc, reported 2015-10-21, distributed nationwide. Cross Contamination With Other Products: Potential cross-contamination of cephalosporin.
| Recall number | D-0013-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Midway Importing, Inc, Houston, TX, United States |
| Recall initiated | 2015-09-22 |
| Classified | 2015-10-13 |
| Reported by FDA | 2015-10-21 |
| Terminated | 2016-08-02 |
| Distributed | Nationwide (US) |
| Quantity | 164,332 boxes |
| UPC / GTIN / UDI-DI | 00188436000174 |
| Lot numbers | 01/17, M51196, M51197, M51198 |
Product
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.
Reason for recall
Cross Contamination With Other Products: Potential cross-contamination of cephalosporin.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0013-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.