READ THIS NEXT: If You Drank This Popular Beverage, Call Your Doctor Immediately, FDA Warns. Besides being effective, part of relying on OTC medicines to treat your ailments is knowing that what you’re taking is safe. Unfortunately, just like food and beverage products, drugs can sometimes fail to meet specific requirements or face contamination issues that require them to be removed from stores and medicine cabinets. On June 16, the U.S. Consumer Product Safety Commission (CPSC) announced a recall of two types of Kroger-brand acetaminophen and Walgreens-branded acetaminophen, which is the generic name for the OTC pain killer commonly known brand, Tylenol. The stores pulled the pills from shelves because they violated the Poison Prevention Packaging Act (PPPA), which requires drugs like acetaminophen to be sold in child-resistant packaging for safety reasons. But it’s not just pain relievers that have been affected. On June 9, the FDA announced Green Pharmaceuticals Inc. had voluntarily recalled certain SnoreStop NasoSpray products after discovering they were contaminated with Providencia rettgeri bacteria, posing a serious health risk for immunocompromised people. And on June 7, Buzzagogo Inc. announced it was voluntarily recalling one lot of its Allergy Bee Gone for Kids Nasal Swab Remedy after FDA testing found that some of the products contained higher levels of yeast and mold than is acceptable. But now, another major pharmacy chain is pulling products from its shelves for safety reasons. On June 21, the FDA announced that Vi-Jon, LLC was voluntarily recalling one lot of CVS Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor it produced for the pharmacy chain. According to the notice, the affected item comes packaged in a 10-ounce clear, round plastic bottle printed with the batch number 0556808 expiration date 12/2023 on the shoulder. The recall notice clarifies that the recalled product was distributed to CVS drug store locations nationwide.
RELATED: For more up-to-date information, sign up for our daily newsletter. According to the FDA, the company issued the recall after samples of the medication sent to a third-party lab tested positive for the bacteria Gluconacetobacter liquefaciens. The microorganism poses a severe risk to immunocompromised patients who consume it, with the agency warning that it “could lead to serious, life-threatening adverse health consequences.“ae0fcc31ae342fd3a1346ebb1f342fcb Fortunately, no health complications related to the recall have yet been reported. But the FDA advises anyone who purchased the laxative to stop using it immediately and return it to the place of purchase immediately. Any customers with questions can contact Vi-Jo by emailing [email protected] on weekdays from 7:30 a.m. to 4:30 p.m. Central Time. Patients who feel they may be experiencing a health problem related to the recalled product should contact their doctor or healthcare provider immediately. READ THIS NEXT: This Popular OTC Drug Can Easily Cause “Severe Damage,” Doctor Warns.
