Massive eye drop recall reflects ongoing issues with manufacturing and FDA inspection

A California company has recalled more than 3.1 million bottles of lubricating eye drops because it had not properly tested—and thus could not prove—whether the products were sterile. These products are sold under several names at major retailers across the country. The company, K.C. Pharmaceuticals, initiated the recall on March 3, 2026.

This article was originally published on MedicalXpress.com

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