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Amprol 25% Medicated Article
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DRUG RECALLLOW

Amprol 25% Medicated Article

Huvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.

What to do

Check the product packaging for lot number and expiration date information. If this information is missing, do not use the product and contact the manufacturer for further instructions.

Recalled
Listed
Updated
Agency
FDA
Firm
HUVEPHARMA EOOD
Recall ID
98712
Status
ONGOING

Recall at a glance

Quantity recalled
241 bags @ 50.0 lbs each, 12,050.0 lbs

Why it was recalled

Huvepharma is recalling one bag of Amprol 25% (amprolium) Type A medicated article due to missing lot number and expiration date information on the product packaging.

Is mine affected?

Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.

AMPROL 25% (amprolium), Type A medicated article, Net Wt.: 50lb (22.68 kg), Manufactured by: HUVEPHARMA, INC., St Louis, MO 63116, Distributed by: HUVEPHARMA, INC., Peachtree City, GA 30269. NADA# 012-350. (Intended for use in chickens, turkeys, and pheasants.) NDC#: 23243-9561-5.

Lot code
XSC442, 30Jun2028, 956150

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-06-11 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification