suave hand sanitizer spray recall

9 hand sanitizers recalled due to toxic chemical Avoid These 115 Hand Sanitizers, F.D.A. Warns - New York Times Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. Superfy - Superfyshop First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. Pickup & Same Day Delivery available on most store items. SUAVE 500ML Professional Pump Hand sanitizer Recommended use Use as a hand sanitizer. 74721-0020-9, 71120-112-01 74721-0020-1 Hand sanitizers recalled by FDA because they might be toxic with 74046-001-18 Benzene is a petrochemical often found in vehicle emissions. FDA updates on hand sanitizers consumers should not use FDA encourages health ce professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAs MedWatch Adverse Event Reporting program (please provide the agency with as much information as possible to identify the product): [7-2-2020] FDA is warning consumers and health care providers that the agency has seen a sharp increase in hand sanitizer productsthat are labeled to contain ethanol (also known as ethyl alcohol) but that have tested positive for methanol contamination. This hand sanitizer formula can be used on hands when soap and water are not available to clean hands and has no added fragrance. . 74046-001-20. If soap and water are not readily available, theCenters for Disease Control and Prevention(CDC) recommend consumers use an alcohol-based hand sanitizer that contains at least 60 percent ethanol (also referred to as ethyl alcohol). Unilever in late March recalled two Suave 24-hour protection aerosol antiperspirants after an internal review found slightly elevated levels of benzene in some samples. (118 mL) Helps reduce harmful bacteria on skin. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. 55028-006-01 75821-002-03. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. 74721-0010-4 Hand sanitizer product packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 6/17/2021, product recalled on 06/21/2021. Suave Hand Sanitizer. . 80969-010-06 Hand Sanitizers Sold At Walmart and Target Are Among Five Recalled 80969-010-07 74721-0020-5 product voluntarilyrecalledon 11/30/2021, Product labeled to contain methanol; FDA recommended the company recall on 12/6/2021; product voluntarily recalled on 12/6/2021, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality even after receiving a warning letter. Call Poison Help at 800-222-1222 to connect to your local poison center. FDA encourages health care professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAs MedWatch Adverse Event Reporting program (please provide the agency with as much information as possible to identify the product): The following chart outlines the information on hand sanitizer labels for consumers to use to identify a product that: FDA advises consumers not to use hand sanitizers produced by the manufacturers identified in the table below. Company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality and scope of contamination. Company tested product; Product labeled as containing Isopropyl Alcohol determined to contain undeclared ethyl alcohol at sub-potent concentrations; FDA recommended the company recall on 2/16/2022 Associated lot numbers: Company tested product lot 200423322; Product labeled as containing Isopropyl Alcohol determined to contain undeclared ethyl alcohol at sub-potent concentrations; FDA recommended the company recall on 2/16/2022. Health Canada issued a mass hair product recall over the detection of the cancer-causing chemical benzene. PRODUCTS. item 3 Honest Hand Sanitizer Spray - Case of 20, 2oz Pump Top Bottles Honest Hand Sanitizer Spray - Case of 20, 2oz Pump Top Bottles. 78378-666-07 [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 11/10/2020; added manufacturer to, Product purported to be made at the same facility that produced an subpotent product; FDA recommended the company recall on 11/10/2020; added manufacturer to, Protec Hands Antibacterial Gel Topical Solution Non-sterile Solution, Smart Care hand sanitizer packaged in 0.84 fl oz. 74721-0001-7 74416-170-08 FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. Suave Hand Sanitizer Kills 99.9% of Germs Alcohol Based Antibacterial Best for dry skin: Sunytizer Hand Sanitizer. Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. Best Spray: Orly Hand Sanitizer Spray. 74721-0002-8 71120-117-02, 75821-001-01 Guangzhou Yilong Cosmetics Co., Ltd. FDA tested product; contains acetaldehyde and acetal contaminants; Company did not adequately respond to FDA requests for records and other information related drug manufacturing, product quality and scope of the contamination. 74721-0002-2 The agency urges consumers not to use these 1-propanol-contaminated products and has expanded its do-not-use list of hand sanitizers at www.fda.gov/unsafehandsanitizers to include hand sanitizers that are or may be contaminated with 1-propanol, in addition to other hand sanitizers the agency is urging consumers not to use. 74046-006-09 This hand sanitizer formula can be used on hands when soap and water are not available to clean hands and has no added fragrance. Suave Hand Sanitizer kills 99.9% of germs. For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. Medline Plus . Flavor Vapors, LLC, dba: Mob Liquid Labs This lightweight hand sanitizer spray dries quickly and leaves hands feeling fresh and clean. 74046-001-05 MVP Sanitizing Services Spray Hand Sanitizer: 76947-198-20 76947-198-21 76947-199-21: . FDA encourages health care professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAs MedWatch Adverse Event Reporting program (please provide the agency with as much information as possible to identify the product): [3/25/2021] FDA is warning consumers and health care professionals not to use Durisan Antimicrobial Solutions Hand Sanitizer manufactured by Sanit Technologies LLC doing business as Durisan in Sarasota, Florida, due to microbial contamination. 79279-421-09 Unit price / per . Product Description Suave Hand Sanitizer kills 99.9 percent of germs. 75612-101-04 FDA recommended the company recall on 06/01/2022. Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%. Back to Questions and Answers Submit your question below: SHOP SAFEGUARD HAND SANITIZER. 74721-0001-6 Generally, all manufacturers and compounders that produce drugs containing ethanol must conduct the limit test for methanol, using the test method that appears in the USP Alcohol monograph. 74046-004-09 79279-520-07 Recall of hand sanitisers (Feb to April 2021) Acure's five-ounce bottle includes moisturizing aloe vera and 70% ethanol to fight both dryness and germs. PDF Safety Data Sheet The FDA has listed 255 different hand sanitizers, mostly produced and distributed in Mexico, that. Home; Hand Sanitizer; Hand Sanitizer Wipes; Featured collection. 1-propanol, not to be confused with 2-propanol/isopropanol/isopropyl alcohol, is not an acceptable ingredient for hand sanitizer products marketed in the United States and can be toxic and life-threatening when ingested. (China), Smart Care Hand Sanitizer Aloe Vera & Vitamin E, 70108-038-01 Learn more at poisonhelp.hrsa.gov/. The Honest Company Hand Sanitizer Spray - Grapefruit Grove - 2 fl oz. Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. Suave hand sanitizer recall - SWIE.com 74046-001-10 The agencys investigation of contaminated hand sanitizers is ongoing. Individuals with compromised immune systems are at increased risk. Proton Armor Antimicrobial Alcohol-Free Foaming Hand Sanitizer. Products that are fraudulently marketed as FDA-approved since there are no hand sanitizers approved by FDA. 79279-520-09 Dove, Suave, TRESemm, other dry shampoo products recalled due to high Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. #937919. Foshan Meixin Biotechnology Co., Ltd.; formerly, Meixin Beauty & Health Care Products Co., Ltd 71120-612-07 80969-010-02 74046-001-17 Masks . FDA expands hand sanitizer recall to at least 75 brands across the U.S. 74046-006-03 FDA remains vigilant and will continue to take action when quality issues arise with hand sanitizers. Has been tested and is found to have microbial contamination. 78378-888-06 Hand Moisturizers; Exfoliators & Scrubs; Body Treatments; Body Powder; Natural Bath & Body; Hand Soap; Hand Sanitizer; Scar & Stretch Mark Treatments; Bath Accessories; Body Sprays; Baby & Children's Bath; Bath & Body for Men; Shop Bath & Body; Sale on Bath & Body; Close menu This testing method can be used to help assure hand sanitizers contain the correct ingredients and do not contain harmful levels of impurities. Herbacil Antiseptic Hand Sanitizer 70% Alcohol, FDA tested product; contains methanol; FDA recommended the company recall on 7/24/2020; product voluntarily, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/24/2020; product voluntarily, Soho Fresh Hand Sanitizer Gel Antibacterial, FDA tested product; contains methanol; FDA recommended the company recall on 9/15/2020; added manufacturer to, SOHO Fresh Hand Sanitizer Gel Antibacterial, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 9/15/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; Product voluntarily recalled by, CALA Advanced Hand Sanitizer with Aloe Vera Extract, FDA-tested product; contains benzene; FDA recommended the company recall Lot 2004718 (Expiration 04/2023) on 12/27/2021; FDA expanded recall on 2/25/2022 to include all hand sanitizer drug products manufactured at the facility; added manufacturer to, Earths Amenities Instant Unscented Hand Sanitizer with Aloe Vera Advanced, FDA tested product; contains methanol; product retained at the border; FDA recommended the company recall of all other potential products on the market on 6/29/2020; added manufacturer to, FDA tested product; contains methanol; FDA recommended the company recall of all other potential products on the market on 6/29/2020; added manufacturer to, Vidanos Easy Cleaning Rentals Hand Sanitizer Agavespa Skincare, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall of all other potential products on the market on 6/29/2020; added manufacturer to, DEPQ Internacional S de RL de CV (Mexico), FDA tested product; benzalkonium chloride level was subpotent; FDA has no evidence this product is in the U.S. market; added manufacturer to, dgreen Advanced Hand Sanitizer Antibacterial Gel, Product purported to be made at the same facility that produced subpotent benzalkonium chloride product; FDA has no evidence this product is in the U.S. market; added manufacturer to, FDA tested product; contains methanol; addedmanufacturerto, Product purported to be made at the same facility that produced methanol contaminated product; addedmanufacturerto, Distribuidora Lagunera del Norte SA de CV (Mexico), FDA tested product; ethyl alcohol level was subpotent; FDA has no evidence this product is in the U.S. market; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA has no evidence this product is in the U.S. market; added manufacturer to, Distribuidora Lagunera del Norte SA de CV, FDA tested product; contains methanol; FDA recommended the company recall on 8/21/2020; added manufacturer to, Cleaner by Crystalware Hand Sanitizer Alcohol Gel, FDA tested product; FDA recommended the company recall on 8/21/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 8/21/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; contains methanol; FDA recommended the company recall on 8/21/2020; added manufacturer to, CleanCare NoGerm Advanced Hand Sanitizer 75% Alcohol, FDA tested product; contains methanol; FDA recommended the company recall on 6/17/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall all other products potentially on the market on 6/17/2020; product voluntarily recalled by, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall all other products potentially on the market on 6/17/2020; added manufacturer to, The Good Gel Antibacterial Gel Hand Sanitizer, CleanCare NoGerm Advanced Hand Sanitizer 80% Alcohol, Estrategia Hospitalaria SA de CV (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 8/5/2020; added manufacturer to, Gaza Proveedora de Servicios de Hospedaje y Alimentacion (Mexico), FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 11/20/2020; product voluntarily recalled on 12/1/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 11/20/2020; product voluntarily recalled on 12/1/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 11/20/2020; product voluntarily recalled on 12/8/2020; added manufacturer to, Genesis Partnership Company SA (Guatemala), FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 8/27/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 8/27/2020; added manufacturer to.