READ THIS NEXT: If You Bought This at Walmart, Stop Using It, Officials Warn After 62 Injuries. Personal hygiene products, toiletries, over-the-counter (OTC) medicines, and personal items are all regulated in the same way that food and beverage items are to ensure safety. And recently, there have been a few cases in which companies have pulled products from the shelves due to a potential health risk.ae0fcc31ae342fd3a1346ebb1f342fcb Earlier this summer, Tennessee-based Vi-Jon, LLC announced a recall of its Magnesium Citrate Saline Laxative Oral Solution. The July 25 notice expanded a previous recall to include all lots of its grape-, lemon-, and cherry-flavored products available for purchase at Rite Aid, Walgreens, CVS, Walmart, Publix, Kroger, and Harris Teeter stores, among other locations. The company pulled the medicine from shelves after third-party microbial testing discovered Gluconacetobacter liquefaciens bacteria, a potentially dangerous microorganism. And on Sept. 16, the FDA announced that Family Dollar had issued a voluntary recall of products it carries that the agency regulates. In one notice, the discount retailer said 41 OTC “medical devices” such as pregnancy tests, contact lens solutions, denture cleaners, denture adhesives, adhesive bandages, condoms, nasal sprays, and personal lubricants were affected. A second notice recalled several Colgate toothpaste and mouthwash products sold by the stores. In both cases, Family Dollar removed the affected items from inventory after discovering they had been “stored outside of labeled temperature requirements.” Now, the agency is warning of another potentially hazardous product. On Sept. 16, the FDA announced that Florida-based Salon Technologies International, Inc., had issued a voluntary recall of one lot of its Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%. The affected products, which were sold on the consumer level, include the lot number 1166A and expiration date 6/18/2023 on the packaging. According to the agency’s notice, the product was distributed in the Seattle, Washington area. It also specifies that 512 bottles of hand sanitizer are affected by the recall. RELATED: For more up-to-date information, sign up for our daily newsletter. The FDA reports that the company decided to issue the recall after firm lab testing found that the hand sanitizer contained benzene, which is classified as a carcinogen. According to the agency, people can be exposed to the cancer-causing chemical by inhalation, swallowing it, or applying it to the skin. It can then cause “cancers including leukemia, and blood cancer of the bone marrow and blood disorders which can be life-threatening” that depends on the duration and level of exposure to the carcinogen. The FDA reports that so far, Salon Tech International has not received any reports of adverse effects from customers using the product. However, anyone who believes they may have experienced problems related to the item should contact their doctor or healthcare provider immediately. The health agency advises anyone who purchased the affected product to stop using it and return it to where it was purchased. The company reports that it has reached out to its distributors to arrange for the return of the items. In addition, customers with questions about the hand sanitizer recall can reach Salon Technologies International by phone or email using the contact information posted in the FDA’s notice.
