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News-Medical.Net on MSNNovel deep learning model leverages real-time data to assist in diagnosing nystagmusArtificial intelligence is playing an increasingly vital role in modern medicine, particularly in interpreting medical images ...
Feast your eyes on one of the most eye-catching diecast model collections featuring stunning motorcycles and cars! From intricate detailing to rare finds, this showcase is a must-watch for ...
For people diagnosed with macular telangiectasia type 2 (MacTel)—a rare and slowly progressing retinal disease—there have ...
If you suffer from dry or itchy eyes, listen up: more than 75,000 cases of eye drop solution were voluntarily recalled nationwide by BRS Analytical Service, a pharmaceutical testing lab ...
The recalled products, which include eye drops and artificial tears, were distributed nationwide over the course of two years. Here's what Illinois consumers should know. St. Louis-based firm BRS ...
AvKare did not specify what issues had been identified. The five recalled products include lubricant eye drops and eye gels, which consumers should immediately cease using, AvKare warned.
Eye care products, including artificial tears and drops, are being recalled by their distributor. The recall responds to deviations from good manufacturing practices discovered during a U.S. Food ...
An eye drop manufacturer has announced a voluntary recall of certain dry eye drops after an audit from the U.S. Food and Drug Administration found "manufacturing cGMP deviations," and has advised ...
Over-the-counter ophthalmic products were voluntarily recalled due to a manufacturing deviation discovered during a U.S. Food and Drug Administration audit, a notice says. Pharmaceutical ...
Nearly 76,000 cases of eye drops have been recalled nationwide by BRS Analytical Services, a pharmaceutical consulting firm, according to an FDA enforcement report. The urgent recall follows an ...
Tens of thousands of cases of eye drops have been recalled by BRS Analytical Services. The recall was initiated on April 23, but the Food and Drug Administration listed it as a Class II on May 6, ...
(WJW) – Multiple over-the-counter eye care products are being voluntarily recalled nationwide after a U.S. Food and Drug Administration audit revealed serious manufacturing violations.
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