Thousands of cases of ophthalmic products were voluntarily recalled after a manufacturing deviation identified during an inspection from the FDA.

More than 75,000 cases comprising more than 1.8 million cartons of consumer level dry eye drops have been voluntarily recalled.

Several types of eye drops sold nationwide have been recalled due a manufacturing issue which can cause a health hazard ...

Multiple over-the-counter eye care products are being voluntarily recalled nationwide after an FDA audit revealed serious ...

The issue was discovered during an audit by the FDA and impacts certain eyedrops sold between May 2023 and April 2025.

Tens of thousands of cases of eye drops have been recalled by BRS Analytical Services. The recall was initiated on April 23, ...

BRS Analytical Services, LLC, a pharmaceutical testing laboratory, had issued a nationwide recall on April 23 to over-the-counter ophthalmic products.

According to the FDA, over 75,000 cases of five different eye drops and artificial tears were recalled. Here's what you need ...

More than 70,000 cases of ophthalmic products are being recalled for manufacturing deviations, according to a press release by distributor AvKARE. The recalled products, which include eye drops and ...

The recall was issued voluntarily following an audit that discovered the manufacturing error that required the recall to be ...

The pharmaceutical testing lab BRS Analytical Service recalled products used to relieve dry and irritated eyes after ...

More than 76,000 eye drops and other eye care products are being voluntarily recalled after an audit by the Food and Drug ...