FDA recalls two more eyedrops due to contamination risks

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FDA recalls two more eyedrops due to contamination risks

U.S. health officials are alerting consumers about two more recalls of eyedrops due to contamination risks that could lead to vision problems and serious injury.

The announcements follow a recall last month of eyedrops made in India that were linked to an outbreak of drug-resistant infections. One person died and at least five others had permanent vision loss.

The recall affects nearly 2,900 bottles, according to the company. The drops were manufactured in Arizona.

Last week, the FDA posted a separate recall announcement from Apotex recalling six lots of prescription eyedrops used to treat a form of glaucoma. The company said it launched the recall after finding cracks in some bottle caps.

The drops are distributed as Brimonidine Tartrate Ophthalmic Solution. 0.15 percent and were sold between last April through February.

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