Apply enough Hand sanitiser gel on your palm. SINGAPORE 159545, AsepsoProfessional Hand Sanitiser (Batch: B42M), Epi KleenGel Hand Sanitizer Gel (all batches), Guardian Lavender & Passion Flower Antibacterial Hand Sanitiser (Batch: 9K28DF), Guardian Aloe & Korean-Mint Antibacterial Hand Sanitiser (Batch: 0D32DF), Kundal Fresh Water Hand Sanitizer+ (Batch: BN227), Sanitelle Instant Hand Sanitizer Antiseptic Gel Kids (all batches), Cath Kidston Moisturising Hand Sanitiser (all batches), Redmoon Bacteriostat Wash Free Hand Wash Gel (all batches), We11 Daily Instant Hand Sanitiser (all batches), Cool Days Peppermint Instant Hand Sanitizer (all batches), Walch Instant Hand Sanitizer (Batch: TG01), Lifebuoy Instant Hand Sanitizer (Batch: OD13UL), FairPrice Hand Sanitiser Lavender (Batch: 201251-001), germ-X Advanced Hand Sanitizer Original Scent (all batches), Sanigen Gel Hand Refreshing Gel 600ml (all batches), Yuri Hand Gel Green Tea Extract (all batches). Blumen products. Target's Born Basic and Walmart's Scent Theory bring the expanded list of recalled sanitizers to more than 75. UNILEVER ASIA PRIVATE LIMITED. Zorin Pharmaceutical Technology Co. Ltd. (China), 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 10/12/2022, Biotipo Pharma Medical Sanitizing Hand Wipes, PalmShield Hand Sanitizer Gel with Aloe and Coconut Oil. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. FDA recommended the company recall on 06/01/2022. Young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk. Aminomethyl propanol isn't really toxic itself, but can be contaminated with nitrosamines which are carcinogenic in nature. 71120-611-08 Children are particularly at risk with these products since ingesting only a small amount of hand sanitizer may be lethal in a young child. (Nevada), Mob Liquid Alcohol Antiseptic Hand Sanitizer Non-Sterile Solution, FDA tested product; isopropyl alcohol level was subpotent; FDA recommended the company recall on 10/13/2022, Salon Technologies International 74530-013-06 The Good Gel Antibacterial Gel Hand Sanitizer. 74721-0020-1 Deep Cleansing. 74721-0001-9 Skin or eye exposure to 1-propanol can result in irritation, and rare cases of allergic skin reactions have been reported. 75821-001-02 Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. 80969-020-03 74721-0002-3 Hand sanitizer to help reduce bacteria that potentially can cause disease. 74530-013-08, 74530-012-01 Hand sanitizer. If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. Klar and Danver Instant Hand Sanitizer. 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. HUMAN OTC DRUG. 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. 74530-012-05 FDA is not aware of any adverse events related to Durisans hand sanitizer products. 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. A asiafrenz High Supremacy Member The date of recall is from February to April 2021. 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. Grapefruit Extract, 74721-0010-1 (But there is no need to be concerned if your children eat with or lick their hands after using hand sanitizer.). Wholesale-level recall of hand sanitisers due to detection of acetaldehyde and/or methanol at levels above the pharmaceutical pharmacopoeia limit. Need help now? FDA recommended the company recall all drug products on 12/12/2022. Product Information. 71120-612-07 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. Instant Sanitizer is the ultimate convenience, one spray easily covers the entire hand. Target and Walmart issued recalls Tuesday for two potentially toxic hand sanitizers that were sold in stores and online. 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). Bio-Odeur. Ethanol used to manufacturer hand sanitizer products under FDAs temporary policies should contain no more than the interim methanol impurity level of 630 ppm to be consistent with those policies. an essential oil, such as tea tree oil or lavender oil, or you can use lemon juice instead. #06-13/14 [emailprotected] Health & Hygiene. FairPrice Hand Sanitiser Lavender (Batch: 201251-001) 16. germ-X Advanced Hand Sanitizer Original Scent (all batches) 17. Dettol Instant Hand Sanitizer. 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). Use of this contaminated hand sanitizer by health care professionals who tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization or extend an existing hospitalization. The agencys investigation of contaminated hand sanitizers is ongoing. A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. Stop supplying specified batches of the product and return the remaining stocks to the company. The new additions contain a. alcohol gel. LIFEBUOY HAND SANITIZER alcohol gel: Product Information: Product Type: HUMAN OTC DRUG: Item Code (Source) NDC:73931-006: Route of Administration: TOPICAL: . 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 09/27/2022; product voluntarily recalled on 9/27/2022. Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. This link opens a new browser tab . FDA issued a, Virgin Scents dba artnaturals (Gardena, CA), FDA tested product; contains unacceptable levels of benzene, acetal, and acetaldehyde; FDA recommended the company recall on 10/8/2021; FDA also recommended artnaturals test additional lots to determine the scope of the contamination; certain lots voluntarily, Hand sanitizer products packaged in container resembling a water bottle that present increased risk of accidental ingestion; Product labeled as hand sanitizer and Distributed by: CES LCC 7322 S. Rainbow Blvd. 74721-0020-7 74721-0020-5 For more information, visit Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? Class 2: For recalls of products with issues that would not likely cause serious adverse health outcomes. 75339-751-03 But according to the FDA, some of the hand sanitizers on the market contain a toxic ingredient -- methanol -- that is dangerous when ingested or absorbed through the skin, and can be fatal in large quantities. 74721-0010-7 These may be signs of a serious condition. Inactive ingredients. 74721-0020-6 Short-term exposure to acetaldehyde can cause irritation to eyes, skin, and respiratory tract while repeated exposure to methanol vapour may cause inflammation of the eye, headaches, giddiness, insomnia, stomach disturbances, and visual failure. Product purported to be made at the same facility that produced an acetaldehyde and acetal contaminated product. Sophora Extract CleanCare NoGerm Advanced Hand Sanitizer 80% Alcohol. Product purported to be made at the same facility that produced product containing acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. This makes rubbing alcohol unpalatable for human consumption. 75339-751-04 Purifying. FDA encourages health care professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAsMedWatch Adverse Event Reportingprogram (please provide the agency with as much information as possible to identify the product): [8/7/2020] Today, FDA issued updated guidances to provide additional clarification on testing of alcohol used in hand sanitizers manufactured under FDAs temporary policies to help ensure that harmful levels of methanol are not present in these products. 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. Mint Oil 74530-012-06 Directions. 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. FDA remindsconsumersto wash their hands often with soap and water for at least 20 seconds, especially after going to the bathroom; before eating; and after coughing, sneezing or blowing ones nose. Filter products Instant Hand Sanitizer (Batch: TG01) Whealthfield s Lohmann (S) Pte Ltd Acetaldehyde 13 TP 706 Hand Sanitiser (Exp: 10/3/2022) Topseller Pte Ltd Acetaldehyde and methanol 14 Lifebuoy Instant Hand Sanitizer (Batch: OD13UL) Unilever Singapore Pte Ltd Acetaldehyde 71120-112-06 [10/4/2021]FDA has tested certain artnaturals scent free hand sanitizer labeled with DIST. 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. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Additionally, FDA reminds consumers that no drugs, including hand sanitizers, are approved to prevent the spread of COVID-19. FDA reminds consumers to wash their hands often with soap and water for at least 20 seconds, especially after going to the bathroom; before eating; and after coughing, sneezing, or blowing ones nose. Products. 74530-013-03 If swallowed, get medical help or contact a Poison Control Center right away. The Health Sciences Authority (HSA) of Singapore has recently recalled 18 sanitizers, this includes products from Lifebuoy, Walch, Guardian and more. Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. View more View less. Topical Solution. Lifebuoy Hand Sanitizer is the most convenient and instant way to hygienic hands. 80969-020-04 Notice to manufacturers and distributors: If you believe your products are no longer within the labeled expiry period, are no longer in distribution, or you otherwise have information that your products no longer warrant inclusion on this list, you should provide your reasoning and supporting information for FDAs consideration toHSDoNotUseListInquiries@fda.hhs.gov. Modesa Instant Hand Sanitizer Moisturizers and Vitamin E. CleanCare NoGerm Advanced Hand Sanitizer 75% Alcohol. Route of Administration. 74721-0010-2 Since the 1950s, it's been added to hand sanitizers, toothpastes, cookware, gardening tools, clothes, toys, furniture, and even some baby teething products. Wat is the side effect.? distilleries that manufacture their own hand sanitizer from alcohol they produce) and do not procure it from an outside source. Safety Information In addition, a Cosmetic Ingredient Review (CIR) expert scientific panel states that benzophenone and its derivatives (benzophenone-1, -3, -4, -5, -9 and -11) are safe as typically used in cosmetics and personal care products. 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. by artnaturals Gardena, CA 90248 and found unacceptable levels of benzene, acetaldehyde, and acetal contaminants. The agency also included an additional denaturant formula in the temporary guidances. 74530-011-08, 74530-013-01 Lifebuoy Instant Sanitizer contains 70% alcohol. 80969-010-07 The level of product recall will depend on the potential hazard of the affected product, extent of distribution and whether other mitigating measures can be taken to address the issue. Fast and effective when there's no time for hand washing. Lifebuoy Hand Sanitizer - 75% Ethyl Alcohol. We11 Daily Instant Hand Sanitiser All batches: Cool Day's Peppermint Instant Hand Sanitizer All batches: Walch Instant Hand Sanitizer TG01: TP 706 Hand Sanitiser Exp: 10/03/2022: Lifebuoy Instant Hand Sanitizer: OD13UL: FairPrice Hand Sanitiser Lavender 201251-001: germ-X Advanced Hand Sanitizer Original Scent All batches: Sanigen Gel . Protects against 99.9% of germs and is proven to be effective against Covid-19 Coronavirus. Sol-m Instant Hand Sanitizer : Alcohol: Gel: Topical: Sol-millennium Medical Inc: Human Otc Drug: 73720-0236: Sol-m Instant Hand Sanitizer : Alcohol: Gel: Topical: Sol-millennium Medical Inc: Human Otc Drug: 73720-0500: Sol-m Instant Hand Sanitizer : Alcohol: Gel: Topical: Sol-millennium Medical Inc: Human Otc Drug: 73720-1000: Sol-m Instant . It not only kills 99.99% germs instantly, but also boosts you immunity for upto 10 hours. Sophora Extract 74530-012-08, Ningbo Pasco UnitedIndustry Co., Ltd.(China), Pasco Instant HandSanitizer Aloe &Moisturizers, Safe Cleaner Hand Sanitizer Gel Has been tested and is found to have microbial contamination. Modesa Instant Hand Sanitizer Moisturizers and Vitamin E. Hello Kitty by Sanrio Hand Sanitizer. Antibacterial, antimicrobial hand sanitizer to help fight germs and bacteria. 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. 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. FDA recommended the company recall on 9/14/2022; product voluntarily recalled on 9/17/2022. Certain hand sanitizers that may not contain a sufficient amount of ethyl alcohol or isopropyl alcohol. Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. The Health Science Authority (HSA) has announced a wholesale-level recall of hand sanitisers. Proton Armor Antimicrobial Alcohol-Free Foaming Hand Sanitizer. The FDA has advised consumers not to use this hand sanitizer. This will help ensure widespread access to alcohol-based hand sanitizers that are free of contamination. 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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In containers resembling a water bottle that presents increased risk of accidental lifebuoy instant hand sanitizer recall ; FDA recommended company!
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