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Please Wear Shoes at Your Medical Manufacturing Job

Barefoot workers and falsified test results were revealed at the Indian plant responsible for recalled eyedrops sold in the U.S.

Yaroslav Shuraev
Yaroslav Shuraev

According to a recent AP article, Indian manufacturer Kilitch Healthcare India, responsible for the recalled eyedrops sold in the U.S., faces significant sanitation and manufacturing issues, including barefoot workers, cracked floors, and altered records. A preliminary inspection report by the U.S. FDA revealed numerous problems at the Mumbai plant, which produced over two dozen eyedrop varieties subject to an FDA safety warning.

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Break out of the ordinary: see what’s new in life sciences packaging
Medical Device Innovations Report
Cutting-edge packaging technologies are transforming the medical device sector in PMMI’s “Innovation in Medical Device” report, featuring advanced materials, smart solutions, and evolving regulations. Editors share insights from nearly 300 PACK EXPO booth visits—each product deemed new and truly innovative—alongside video demonstrations of the equipment and materials on display.
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Medical Device Innovations Report