40,000 bottles of eye drops across the US recalled over issues with sterility of product
Prestige Brand Holdings has issued a voluntary recall for nearly 40,000 bottles of Clear Eyes Maximum Itchy Eye Relief drops due to sterility concerns. The FDA has classified this as a Class II recall, advising consumers to stop using the product and seek a refund.
Why it matters
Product recalls involving medical supplies highlight ongoing safety oversight challenges in the pharmaceutical supply chain.
The FDA classified the action as a Class II recall, defined on the agency’s website as a moderate-risk situation. The FDA classified the action as a Class II recall, defined on the agency’s website as a moderate-risk situation. Product recalls 40,000 bottles of eye drops across the US recalled over issues with sterility of product Prestige Brand Holdings has voluntarily recalled a batch of its Clear Eyes eye drops after FDA alert
Prefer the Guardian on Google Nearly 40,000 bottles of eye drops are being pulled from store shelves across the US over concerns about potential contamination, according to the Food and Drug Administration (FDA).
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