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Eyedrops that have been recalled may contain a “bacteria” strain linked to blindness and eye injuries, according to US health officials

Photo EzriCare

In January and February, two eye drop brands were pulled from shelves after being linked to a drug-resistant bacteria strain that has been blamed for at least one fatality and numerous serious health issues. In January, the CDC issued a caution urging people to stop using artificial tears made by Delsam Pharma and EzriCare. The following month, Global Pharma, the firm that owns the brands, announced a voluntary recall in response to an official FDA recommendation.

An uncommon strain of bacteria found in the recalled eyedrops has been linked to numerous infections, instances of vision loss, surgical removal of the eyeballs, one fatality, and dozens of infections. Global Pharma was forced to recall eye drops in February after they were linked to a drug-resistant bacteria strain that was responsible for at least one fatality.

The US Centers for Disease Control and Prevention discovered 68 patients in 16 states with infections brought on by a rare strain of Pseudomonas aeruginosa that was drug-resistant and had never been reported in the nation in a report published this week. The CDC observed that the majority of patients used fake weeping. EzriCare Artificial Tears were the ones that were cited the most by patients, despite the fact that they had used other products as well.

The urinary, respiratory, and corneal tracts illnesses have been recorded as adverse events as of March 14. There have been four accounts of eyeball removal surgery and eight complaints of vision loss. One death was initially stated as having occurred. Consumers who have recalled products are urged not to use them any longer by the CDC and US Food and Drug Administration.

Due to a possible bacterial infection, the FDA recommended on February 22 that Global Pharma recall Delsam Pharma’s Artificial Eye Ointment. Global Pharma followed suit. Pharmedica USA is recalling two batches of its anti-inflammatory Purely Soothing 15% MSM Drops due to “non-sterility,” the FDA stated on March 3. The company stated that it had not been made aware of any sickness or unfavorable product-related incidents. Apotex is recalling six samples of brimonidine tartrate ophthalmic solution 0.15%, a prescription eye drop used to treat open-angle glaucoma or ocular hypertension.

A Florida lady launched a lawsuit against the pharmaceutical company last week, claiming that one of her eyes had to be removed due to an infection she acquired after using their product. According to the CDC, testing showed that the bacteria were found in opened bottles taken from patients. Unopened packages are currently being examined to determine whether manufacturing-related contamination has occurred.

CWEB has provided some information for this story.

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