Reported May 27, 2026 · Ongoing

Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by

Zydus Pharmaceuticals (USA) Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zydus Pharmaceuticals (USA) Inc · 73 Route 31 N · Pennington, NJ · 08534-3601

Is this the product you have?

Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by

3 of 3 products

Products covered by this recall
#Product as published
1Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534
230 count bottles (NDC 70710-1047-3)
3100 count bottles (NDC 70710-1047-1).
Lot codes and dates
  • Lotsa) M411146
  • Expires
    • 08/2026
    • M502098
    • M502097
  • Expires
    • 01/2027
    • b) M411145
  • Expires08/2026
Amount recalled
23,880 bottles

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 4:18 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.