Cetirizine recall over ranitidine contamination
Analysis based on 7 articles · First reported Jul 21, 2026 · Last updated Jul 23, 2026
The recall is limited in scope and no adverse events have been reported, so market impact is minimal. However, it may raise concerns about manufacturing quality at KC Pharmaceuticals and its subsidiaries.
Unique Pharmaceutical Laboratories, a division of KC Pharmaceuticals, voluntarily recalled four lots of Cetirizine Hydrochloride Tablets USP 5 mg (generic Cetirizine) due to possible cross-contamination with ranitidine (generic Zantac). The recall was prompted after a pharmacy technician noticed red dots on tablets. The FDA published the recall announcement on July 20, 2026. No adverse events have been reported. The affected lots were distributed nationwide by Rising Pharmaceuticals The contamination could cause life-threatening allergic reactions in sensitive individuals.
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