Amazon voluntarily withdraws 7 cases eye drops The brand was taken off shelves in response to a warning letter issued by the Food and Drug Administration about potential safety concerns.
According to the FDA, the eye drops, which are sold as a homeopathic treatment for dry eyes, cataracts, and inflammation caused by dust and other allergens, are considered “new drugs” that have not yet been formally approved for sale by the FDA. Masu. Warning notice.
A warning letter will be sent after the agency: Recall batch for eye drop products over- In recent weeks, Including over 2 dozen Eye drop products sold by CVS Health, Leader (Cardinal Health), Rugby (Cardinal Health), Rite Aid, Target, Velocity Pharma and Walmart were recalled “due to unsanitary conditions found by FDA investigators,” USA said. Today previously reported report.
Other eye drop products have been recalled once in the past month. August and another time February Due to the potential for contamination, infection, vision loss, minority deaths, and other adverse conditions, CNN report.
Online retail giants have already begun the process of removing traces of these products from their sites.
“Safety is our top priority at Amazon. All products offered in our store must comply with applicable laws and regulations. The product in question has been investigated and is in the process of being removed,” a company spokesperson said. said the person. With CNN.
Here’s what we know:
caveat:FDA recalls 27 more eye drops: What you need to know as a consumer
What eye drop products has Amazon voluntarily recalled?
According to the FDA, the sale and distribution of these ophthalmic products is of particular concern because “the route of administration of these products bypasses some of the body’s natural defenses,” creating a greater risk of harm. It is said that it is a thing.
The recalled products are “not generally recognized as safe and effective” based on their intended use labeling.
Therefore, they are classified as “new drugs” by the FDA. Without an application for approval from the FDA, a new drug cannot be introduced into interstate commerce or shipped for introduction.
The list of recalled products is as follows:
- Simila Sun Pink Eye Relief
- Goodbye Company Pink Eye
- Can-C eye drops
- Optique 1 eye drops
- occlumed eye drops
- TRP Natural Eyes Floaters Relief
- Manzanilla Sofia Chamomile Herbal Eye Drops
What should I do if I have already ingested the product?
FDA recommends that consumers contact their health care provider or seek immediate medical attention if they experience any signs or symptoms of a potential infection.
Side effects to eye drops, such as discharge, redness, or pain, may indicate an infection. People should also check the expiration date on products before using them, said Dr. Christopher Starr, a spokesperson for the American Academy of Ophthalmology. Shared with CBS.
Consumers should also dispose of eye drop products properly according to guidelines set by the government. F.D.A. Users of eye drop products who have experienced a severe reaction as a result of the recalled product should Report online With the F.D.A.
Eye drops recall list:See dozens of eye care products to be recalled in 2023
