If you get this common over -the -counter medication at CVS, stop using it now, the FDA warns
The agency warns that pills may have a major health risk for some people.
Having over -the -counter medication (OTC) can facilitate the resolution of any minor health problem that occurs in your daily life. And you take a pill to fight against sudden indigestion or you are looking forrelief of evils and pain, there is a decent chance that you have visited your local pharmacy to recover them. But if you recently recovered over-the-counter medicines in CVS, you may want to take a minute to check if this is part of a reminder that the Food & Drug Administration (FDA) has just issued. Read the rest to see which product the pharmacy chain draws shelves due to a serious security problem.
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There has recently been a series of reminders on popular OTC drugs.
In addition to being effective, part of relying on over -the -counter medicines to treat your ailments is knowing that what you are taking is sure. Unfortunately, just like food and drinks, drugs may sometimes not meet specific requirements or face contamination problems that require that they are withdrawn from pharmacy stores and cupboards.
On June 16, the U.S. Consumer Product Safety Commission (CPSC) announced a reminder of two types ofKroger brand acetaminophen And the Walgreens brand acetaminophen, which is the generic name of the over -the -counter, Tylenol bread bread brand. The stores have pulled the shelves because they have violated the law on poisons prevention packaging (PPPA), which requires drugs such as acetaminophen to sell in children's resistant packaging for safety reasons.
But it is not only the analgesics that have been affected. On June 9, the FDA announced that Green Pharmaceuticals Inc. voluntarily recalled someSnorestop Nasospray products after discovering that they were contaminated byProvidencia Rettgeri Bacteria, posing a serious health risk for immunocompromised people. And on June 7, Buzzagogo Inc. announced that he voluntarily recalled a lot of hisAllergy bee has disappeared for children The nasal swab remedy after the FDA tests revealed that some products contained higher yeast and mold levels than that is acceptable. But now another large pharmacy chain draws products from its shelves for safety reasons.
The FDA has just made a recall of a common CVS CVS drug.
On June 21, the FDA announced thatVi-Jon, LLC remembered voluntarily A batch of CVS magnesium citrate saline laxative lemon solution that it produced for the pharmacy chain. Depending on the notice, the article assigned is packed in a clear plastic bottle of 10 ounces printed with the lot number 0556808 expiration date 12/2023 on the shoulder. The recall notice specifies that the recalled product has been distributed to the locations of CVS pharmacies nationally.
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The company pulled the shelves medication after discovering potential bacterial contamination.
According to the FDA, the company published the recall after the drug samples sent to a third -party laboratory have been tested positive for bacteriaLiquefaciens gluconacetobacter. The microorganism presents a serious risk for immunocompromised patients who consume it, the agency warns that this "could lead to serious and potentially fatal unfavorable consequences".
Here is what you need to do if you have the medication recalled in your office.
Fortunately, no recall health complications have yet been reported. But the FDA advises all those who bought the laxative to stop using it immediately and returned immediately to the place of purchase.AE0FCC31AE342FD3A1346EBB1F342FCB
All customers with questions can contact VI-Jo by sending an email to [email protected] during the week from 7:30 a.m. to 4:30 p.m. Central time. Patients who believe they can encounter a health problem related to the product recalled must immediately contact their doctor or health care provider.
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