The .gov means its official.Federal government websites often end in .gov or .mil. . Between Feb-Apr, however, the Health Sciences Authority (HSA) did a recall of 18 hand sanitiser products, including those from Guardian, Lifebuoy, FairPrice, and Cuticura. Lifebuoy hand sanitizers have 70% alcohol content and are effective against 99.99% of germs. Instant Sanitizer is the ultimate convenience, one spray easily covers the entire hand. Apply enough Hand sanitiser gel on your palm. Purified Water USP, Acrylates Copolymer, Glycerin, Triethanolamine, Aminomethyl Propanol, Set id: 6f83fed4-5dd2-4a48-8ec7-749b01a328f7, 50 mL in 1 BOTTLE; Type 0: Not a Combination Product, 500 mL in 1 BOTTLE; Type 0: Not a Combination Product, 50 mL in 1 TUBE; Type 0: Not a Combination Product, Place enough product on hands to cover all surfaces. Is being recalled by the manufacturer or distributor. Lifebuoy Antibacterial Hand Sanitizer . Company did not respond adequately to multiple FDA requests for records and other information related to drug manufacturing, product quality and questions regarding possibility of methanol contamination which cannot be ruled out; the firm announced a voluntary recall on 10/18/2022. FDA is not aware of any adverse events related to Durisans hand sanitizer products. Call 9-1-1 if the person is unconscious or has trouble breathing. The site is secure. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. Target and Walmart issued recalls Tuesday for two potentially toxic hand sanitizers that were sold in stores and online. Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. Uncategorized. Our experts have done a research to get accurate and detailed answers for you. Products. A hand sanitizer is generally a slightly safer, better-smelling product, and often comes in easily-carried bottles or containers. Sterillium is the classic among the alcohol-based disinfectants for hygienic and surgical hand disinfection. Artnaturals Hand Sanitizer Infused with Jojoba Oil, Germ Free Anti-Bacterial Instant Hand Sanitizer, Apollo Instant Hand Sanitizer Anti Bacterial, Health & Wellness Essentials Hand Sanitizer Wash-Free, New Sanicol Advanced Antibacterial Hand Sanitizer, National Travel Products, Inc (New Jersey), 74530-015-01 75821-002-03. Modesa Instant Hand Sanitizer Moisturizers and Vitamin E. CleanCare NoGerm Advanced Hand Sanitizer 75% Alcohol. The testing method (with appropriate validation) can be used for hand sanitizers labeled with either alcohol (ethanol) or isopropyl alcohol (also called isopropanol or 2-propanol) as the active ingredient and can screen for potentially harmful impurities, as listed in FDAs temporary guidances. While USP has not yet updated the Isopropyl Alcohol Monograph to include a specific methanol limit, FDA may consider the 200 ppm methanol limit for ethanol to also be suitable for isopropyl alcohol. Cultivation Republic (Clearwater, Florida). Soothing. [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. Supervise children under 6 years of age when using this product to avoid swallowing. First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. 80969-020-03 They are found in a wide range of consumer products including hand sanitizers. 74721-0002-9, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 7/12/2022, Safe Cleaner K Skin or eye exposure to 1-propanol can result in irritation, and rare cases of allergic skin reactions have been reported. 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. Kleanz Antibacterial Hand Sanitizer Advanced, Be Safe Hand Sanitizer (labeled with Model: BF-HGXXXX-09 where XXXX changes based on packaging size), Product manufactured at a facility that did not respond to multiple FDA requests for recordsrelated to drug manufacturing and product qualityeven afterreceiving a warning letter. Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? Aminomethyl propanol isn't really toxic itself, but can be contaminated with nitrosamines which are carcinogenic in nature. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Defenz. The policy outlined in this guidance applies to all pharmaceutical alcohol used as an active or inactive ingredient in a drug, including hand sanitizer under the FDAs temporary policies for preparing alcohol-based hand sanitizer during the COVID-19 pandemic. Consumers can easily identify which hand sanitizer products to avoid by using the following information: Distributors may use more than one manufacturer to produce their hand sanitizer products, which are then marketed under the exact same brand or product name. FDAs investigation of methanol in certain hand sanitizers is ongoing. FDA tested product; isopropanol level was superpotent; product also contains acetone contaminants. Purifying. Suite #166 Las Vegas, NV 89139" FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product, Hand sanitizer products packaged in container resembling a water bottle that present increased risk of accidental ingestion;Product labeled as handsanitizer and Distributed by: CES LCC 7322 S. Rainbow Blvd. 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; added manufacturer to, 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. The dangers of drinking any hand sanitizer under any conditions. Company tested product; contains benzene. When using this product keep out of eyes, ears, and mouth. Methanol is not an acceptableingredient for hand sanitizers and must not be used due to its toxic effects. 71120-112-10 The level of recall is classified as a wholesale level recall, which means that the affected products or batches are recalled from wholesale suppliers. Anti-Bac Hand Sanitizer 65% Alcohol, Scent Theory Keep It Clean Pure Clean Anti-bacterial Hand Sanitizer, Cavalry (labeled with Product of Mexico), Natural Gold Gel Alcohol Antiseptic 75% Topical Solution, Command Gel AntiBac Instant hand sanitizer, FDA tested product; contains methanol; FDA recommended the company recall on 7/31/2020; product voluntarily, UltraCruz Hand Sanitizing Gel Antimicrobial, Company tested product; isopropyl alcohol level was subpotent; product voluntarily recalled lot BF12530 on 8/7/2020, Sanit Technologies LLC, doing business as Durisan (Florida), Durisan Antimicrobial Solutions Hand Sanitizer, Alcohol-Free, Company tested product; contains microbial contamination; product, Durisan Antimicrobial Solutions Hand Sanitizing Wipes, Alcohol-Free, New Wave Cleaning Solutions Foaming Hand Sanitizer (Benzalkonium chloride 0.1%), Company tested product; manufacturing process lacks adequate controls to prevent microbial contamination. A recall can also be initiated to remove products with quality defects that does not impact safety or efficacy from the market so as to ensure that products registered in Singapore continue to meet the stringent regulatory standards stipulated by HSA. Wholesale-level recall of hand sanitisers due to detection of acetaldehyde and/or methanol at levels above the pharmaceutical pharmacopoeia limit. Grapefruit Extract, 74721-0001-1 Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 08/16/2022. 74721-0002-1 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). Note: The Health Sciences Authority (HSA) publishes information regarding recalls of health products supplied in Singapore. 74721-0001-0 74530-013-03 Our team has collected thousands of questions that people keep asking in forums, blogs and in Google questions. 74721-0020-0 alcohol gel. Ingesting 1-propanol can cause central nervous system (CNS) depression, which can result in death. Hand sanitizer products packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 09/08/2021. Peak Processing Solutions - Ethanol sanitizer 80%. Proton Armor Antimicrobial Alcohol-Free Foaming Hand Sanitizer. Now, we have got the complete detailed explanation and answer for everyone, who is interested! FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product. Klar and Danver Instant Hand Sanitizer. Hand sanitizer. 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. Protects against 99.9% of germs and is proven to be effective against Covid-19 Coronavirus. A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. The date of recall was between February and April. Drinking even a small amount of hand sanitizer can cause alcohol poisoning in children. These product recalls may be conducted on a companys own initiative or upon HSAs request to remove products where there are issues with quality, safety or efficacy. 74530-011-04 Dettol Instant Hand Sanitizer. FDA tested product; contains unacceptable levels of acetaldehyde and acetal; Company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality and the scope of the contamination; FDA recommended the company recall on 11/29/2022. FDA recommended the company recall on 9/14/2022; product voluntarily recalled lot 1166A on 9/17/2022. FDA test results show certain hand sanitizers have concerningly low levels of ethyl alcohol or isopropyl alcohol, which are active ingredients in hand sanitizer products. Take some flour in a bowl and add some hand sanitizer to it. 75821-001-03 Purified Water USP, Acrylates Copolymer, Glycerin, Triethanolamine, Aminomethyl Propanol. Alcohol-based hand sanitizers that are contaminated with methanol are subject to adulteration charges under the FD&C Act. 71120-611-08 However, consistent with FDAs temporary policies for hand sanitizer prepared during the COVID-19 pandemic, FDA does not intend to take action against firms preparing hand sanitizer under the temporary policies that have not tested each lot of pharmaceutical alcohol for methanol, if the firms use alcohol they have produced themselves (e.g. 74721-0010-2 The agency will provide additional information as it becomes available. This makes Lifebuoy Immunity Boosting Hand Sanitizer your defense against germs without having to make a trip to the wash basin. Moisture infused. Is packaged in a container that resembles a food/beverage container that presents increased risk of accidental ingestion. 74530-015-05 Rp6.000. Consumers who have products on thelist of hand sanitizerswith potential methanol or 1-propanol contamination should immediately stop using the product and dispose of it, ideally in ahazardous waste container. Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. Gentle Protection. A lot has happened since the COVID-19 global pandemic reached the shores of America in 2020. 80969-007-01 Item Code (Source) NDC:50069-103. 70% Alcohol Cleansing Gel Say Goodbye to Germs. Animal studies show acetaldehyde may cause cancer in humans and may cause serious illness or death. Need help now? The test method for methanol described in the USP Alcohol Monograph can also be used to test for methanol contamination in isopropyl alcohol. For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. FDA recommends using the test methods described in the USP monograph for alcohol (ethanol) and conducting the testing in a laboratory that has been previously inspected by FDA and is compliant with current good manufacturing practice (CGMP). 74721-0002-8 Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. These may be signs of a serious condition. 201 HENDERSON ROAD 74721-0001-3 Products packaged to appear as drinks, candy or liquor bottles, as well as products marketed as drinks or cocktails because their appearance could result in accidental ingestion or encourage ingestion. Show More . HAND SANITIZER Isopropyl Alcohol Antiseptic 75% Topical Solution, FDA tested product; contains benzene; FDA recommended the company recall Lot 200324 (expiration date unknown) on 03/30/2022, Product labeled to contain methanol; FDA recommended the company recall on 11/18/2021. Made in Korea. 80969-020-04 75821-001-04 Class 2: For recalls of products with issues that would not likely cause serious adverse health outcomes. In case of contact, rinse eyes thoroughly with water. distilleries that manufacture their own hand sanitizer from alcohol they produce) and do not procure it from an outside source. To date, artnaturals has not responded to multiple FDA attempts to discuss the contaminated hand sanitizers, including identification of the manufacturer, possible recalls, and the scope of the contamination. Godrej Protekt Hand Sanitizer. FDA recommended the company recall on 06/01/2022. HUMAN OTC DRUG. The agency is aware of adults and children ingesting hand sanitizer products contaminated with methanol that has led to recent adverse events including blindness, hospitalizations and death. Gigi's Goodbye Germs Hand Sanitizer. Polyethylene Glycol Compounds (PEGs) are utilized for their thickening, softening, and penetration-enhancing properties. by artnaturals Gardena, CA 90248 and found unacceptable levels of benzene, acetaldehyde, and acetal contaminants. Methanol is not an acceptable ingredient for any drug and should not be used due to its toxic effects. Products labeled with harmful or poisonous ingredients, such as methanol. 74530-011-08, 74530-013-01 74530-013-05 Modesa Instant Hand Sanitizer Moisturizers and . Guangzhou Minghui Cosmetics Co. Ltd. (China), Product purported to be made at the same facility that produced subpotent ethyl alcohol product;added to import alert to help stop products from entering the U.S. on 12/21/2020; FDA recommended the company recall on 4/12/2021; FDA issued awarning letteron 07/06/2021; product voluntarily recalled by Native Promotions, Inc. on 7/12/2021, Guangzhou Orchard Aromatherapy & Skin Care Co., Ltd. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 5/16/2022; FDA issued a warning letter on 07/20/2022. 71120-611-07 [10/4/2021]FDA has tested certain artnaturals scent free hand sanitizer labeled with DIST. To the campus community: The U.S. Food and Drug Administration (FDA) recently recommended a recall of Blumen clear advanced hand sanitizer with 70% alcohol due to the product testing positive for methanol contamination. 74721-0001-4 Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. This is different from a consumer level recall where the products or batches are recalled from patients, consumers, wholesale suppliers, retail suppliers, hospitals, clinics, and pharmacies, or a retail level recall, where products or batches are recalled fromretail suppliers, hospitals, clinics and pharmacies as well as wholesale suppliers. When a recall is initiated, it does not necessarily imply that a product is considered unsafe or is inefficacious. The Good Gel Antibacterial Gel Hand Sanitizer. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. 71120-612-07 This is due to the detection of acetaldehyde and/or methanol at levels that are above the pharmaceutical pharmacopeia limit. 18 Hand Sanitizers Products Recalled Due to Excessive Amount of Methanol: It is recommended to use hand sanitizers with at least 60% ethanol alcohol or 70% isopropanol. UNILEVER ASIA PRIVATE LIMITED. Cosmeticos Ltda, (Brazil), Biotipo Pharma Medical Antibacterial Antiseptic Cleanser Disinfectant, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 10/18/2022, Reborncare Hand Sanitizer (100mL, 250mL, 500mL). Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. 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. 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