Recalls: Personal Care

July 3, 2024 Focusee Recalls Tideway Hair Dryers Due to Electrocution or Shock Hazard

This recall involves Tideway High-Speed Hair Dryers PRO M01 with two speed adjustments. The hair dryers come with a nozzle, and were sold in white with gold on the bottom of the handle. "Tideway" is printed on the front of the handle. The hair dryers have an LED ring on them that corresponds to the different temperature settings of the hair dryer. Red represents hot air, orange represents warm air, blue represents cold air, and green represents hot and cold cycles. Read more.


June 20, 2024 StyleCraft Recalls Instinct Cordless Hair Clippers Due to Fire and Burn Hazards

This recall involves StyleCraft Instinct Cordless Clippers with model number SC607M. The model number and lot number are printed on the back of the recalled clippers. Only the following lot numbers are included in this recall: 35-22, 40-22, 15-23, 20-23, 25-23, 30-23, 35-23, and 40-23. The products were sold in blue, red, and black. The letters "SC" and the name "INSTINCT" are printed on the front cover. Read more.


June 13, 2024 Southern Telecom Recalls Lomi Roll-On Waxing Kits Due to Fire, Burn and Shock Hazards

This recall involves the Lomi Roll-On Waxing Kit with Wax Cartridge & Wax Strips with model number LOMB2003PK. The recalled boxed kits included a handheld wax warmer, a wax cartridge, wax strips, a power cord, and a user’s manual. The Lomi logo is printed on the front of the white and pink warmer, and on the outside of the product packaging. The Lomi logo and model number are on the bottom of the wax warmer. Read more.


February 29, 2024 Nutraceutical Recalls Heritage Store Hydrogen Peroxide Mouthwash Due to Risk of Poisoning; Violation of Child Resistant Packaging Requirement

This recall involves Heritage Store Hydrogen Peroxide Mouthwash in Wintermint and Eucalyptus Mint flavors. The bottles are a dark opaque brown with a white lid. The pink and white label on the front of the bottles displays the Heritage Store logo, product name and flavor. All lots are included in the recall. Read more.


January 4, 2024 Homedics Recalls Massagers Due to Fire and Burn Hazards

This recall involves the HoMedics Therapist Select Massagers with model number HHP-715. The product has a 120 VAC, 60 HZ power cord. "HoMedics" is printed on the side of the barrel of the product. The products are black with a handle, housing and massage head attached to the end. The product has four interchangeable massage heads. Only manufacturing dates through the end of 2022 and prior are included in the recall. The manufacturing date is represented by a date code found on a sticker on the underside of the product's barrel. Date codes are a 4-digit number WWYY where WW is the sequential week of the year and YY is the last two digits of the manufacturing year. Only products with a YY of 20, 21 or 22 are subject to this recall. Read more.


September 28, 2023 Nutraceutical Recalls Solaray Liposomal Multivitamins Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves Solaray Liposomal Women's in 60 and 120 count, Solaray Universal Multivitamin in 60 and 120 count, and Solaray Liposomal Women's 50+ Multivitamin in 120 count. The bottles are a clear silver color with white pop top lids. The white label on the front of the bottles displays the Solaray logo, product name, product type and size count. The 60 count bottles are contained in cartons, which are substantially similar in appearance to the bottles inside. All lots are included in the recall. Name Count SKU Solaray Liposomal Women's 60 076280193251 Solaray Liposomal Women's 120 076280339536 Solaray Universal Multivitamin 60 076280640168 Solaray Universal Multivitamin 120 076280830385 Solaray Liposomal Women's 50+ Multivitamin 120 076280154832 Read more.


June 22, 2023 Nationwide Pharmaceutical Recalls Iron Dietary Supplements Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containing 324 mg of ferrous sulfate (iron) in bottles of 100 tablets. "Nationwide Pharmaceutical" and its logo are printed on the top left of the bottle's label panel. The recalled bottles include lot numbers M0786, M0816, M0817 and M0818, which are printed on the bottom of the bottle. Read more.


May 18, 2023 Acme United Recalls PhysiciansCare Brand Allergy Relief and Cold and Cough Tablets Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold on Amazon.com

This recall involves PhysiciansCare brand Allergy caplets with item number 90036, Allergy Plus tablets with item number 90091, and Cold and Cough tablets with item numbers 90092 and 90033. They are packaged in boxes of 50, 100 and 250 tablets/caplets. The item numbers are printed on the top right corner of the box. The recall includes the following: Item Number Description 90036 PhysiciansCare Allergy; 50 caplets 90091 PhysiciansCare Allergy Plus; 100 tablets Non-Drowsy Cold and Cough; 100 tablets 90033 PhysiciansCare Cold and Cough; 250 tablets Read more.


March 30, 2023 Lexmark Ventures Recalls Solexio Hair Stylers Due to Electrocution or Shock Hazard

This recall involves lithium-ion battery packs and replacement batteries on XS series Pulsator, Swimmer, This recall involves Solexio STYLR Hair Stylers, which can be used to straighten hair. They are black with either a pink or gray colored handle, controls and lock switches with matching color on the power cord. They are approximately 11 inches long, 1.4 inches in diameter and weigh about 14.5 ounces. Product number "78T0100" for pink models and product number "78T0300" for gray models is printed on a black and gray label inside the barrel of the stylers. Affected models have a date code between 147 and 253. The date code is the middle three numbers of the serial number, which starts with 8081. The serial number is located below the product number on the silver and black label inside the barrel of the stylers. Read more.


March 16, 2023 Pfizer Recalls Nurtec ODT Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves prescription drugs Nurtec ODT 75 mg orally disintegrating tablets sold in cartons containing one blister card of 8 tablets. The tablets are in a non-child resistant blister card packaged in a carton that includes the name of the product, dosage strength, expiration date. The dosage strength and expiration date are printed or stamped on the blister card. The recall includes the following: Product Description NDC Number Expiration Date Nurtec® ODT (rimegepant) 75mg 8-Unit Dose blister pack 72618-3000-2 All dates through 6/2026 Read more.