Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Sep 22, 2015 (11 years ago)

Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Cause type: Cross-contamination

Traces of another drug - most often penicillin - got into the product from shared equipment or facilities. Even trace penicillin can trigger a severe allergic reaction in someone who was never meant to receive it. All cross-contamination recalls.

What was recalled

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.

Drug: Acetaminophen Category: Pain Relief & OTC Medication

Recalling firm
Midway Importing, Inc
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0013-2016 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Acetaminophen recalls

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Class II · Moderate risk

Tylenol

Defective Container

Ongoing Packaging defect Kenvue Brands LLC D-0121-2026
Class II · Moderate risk

Acetaminophen 500mg Caffeine 65mg caplets

Labeling: Label Mix-up. This issue affects the outer box labeling only. The box incorrectly states the ingredients Acetaminophen 500mg and Caffeine 65mg. The inner pouch correctly states the ingredients are Aspirin (NSAID)*500mg and Caffeine 32.5mg.

Ongoing Labeling / mix-up Aero Healthcare NDC 55305-135-01 D-0155-2026

Other cross-contamination recalls from 2015

All cross-contamination recalls
Class II · Moderate risk

Mupirocin Calcium Cream

Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.

Terminated Cross-contamination GlaxoSmithKline, LLC. NDC 66993-942-15 D-1362-2015
Class II · Moderate risk

Bactroban Cream

Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.

Terminated Cross-contamination GlaxoSmithKline, LLC. NDC 0029-1527-22 D-1361-2015
Class II · Moderate risk

Bactroban Ointment

Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.

Terminated Cross-contamination GlaxoSmithKline, LLC. NDC 0029-1525-44 D-1360-2015
Class II · Moderate risk

Bactroban (mupirocin calcium)

Penicillin Cross Contamination and Presence of Foreign Substance. Product was contaminated with penicillin and foreign substances during manufacturing process.

Terminated Cross-contamination GlaxoSmithKline, LLC. NDC 0029-1526-11 D-1359-2015