FDAnews Drug Daily Bulletin
Pharmaceuticals / Quality

Mexican Drugmaker Warned for Adulterated Product

Jan. 11, 2018
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The FDA issued a warning letter to Prosana Distribuciones in Mexico City for serious GMP violations and for producing an adulterated drug product.

In a March inspection, the agency found that two batches of the firm’s product, Bicaruvas antacid effervescent powder, were distributed before certificates of analysis were obtained from a third-party testing laboratory.

The facility lacked adequate written procedures to ensure stable drug manufacturing operations and drug quality. The FDA investigators found the firm had not validated its manufacturing processes or performed process qualification studies, and did not have master batch records for each batch size. Three batches were found to contain five times the amount of calcium carbonate stated on the product label.

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