FDA Hand Sanitizer Recall List 2021, Page 2 - SWIE.com 74046-001-08 Certain hand sanitizers are being recalled because they do not meet Health Canada's requirements. 75339-751-05 74046-004-05 FDA updates on hand sanitizers consumers should not use 74721-0001-8 There's a nationwide spray hand sanitizer recall on 11 products that were sold at Ulta, TJ Maxx, and Marshalls stores. distilleries that manufacture their own hand sanitizer from alcohol they produce) and do not procure it from an outside source. 74721-0002-1 74721-0020-0 Health Canada recalls 9 more hand sanitizers over safety risks FDA issued a, Yara Elena de La Garza Perez Nieto (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 7/10/2020; added manufacturer to, Product labeled to be edible alcohol; added manufacturer to. 74046-004-07 Unibeleza Industria E Comercio De 74530-015-03 While hand sanitizers with possible methanol contamination are more life-threatening than those that are not contaminated,FDA urges consumers not to drink any of these products. GSD All Purpose Liquid Sanitizer & Disinfectant MEGA REFILL SIZE 1.75L (59.2 OZ) 80% ALCOHOL GSD All Purpose Liquid Sanitizer & Disinfectant FAMILY SIZE 1L (33.2 OZ) 80% ALCOHOL GSD All Purpose Liquid Sanitizer & Disinfectant POCKET SIZE 375mL (12.6 OZ) 73% Alcohol - Gel Sanitizer & Disinfectant With Essential Oils 73% ALCOHOL FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product; FDA issued a warning letter on 01/30/2023. 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. Keep all hand sanitizers out of the reach of children. FDA updates on hand sanitizers consumers should not use | FDA 71120-112-11 Consumers who have been exposed to hand sanitizer containing methanol and are experiencing symptoms should seek immediate treatment for potential reversal of toxic effects of methanol poisoning. 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. 79279-421-06 ADVERTISEMENT. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. 74046-006-10. 74721-0010-6 While the exact risk from using hand sanitizer containing benzene, acetaldehyde, or acetal is unknown, FDA recommends consumers do not use products contaminated with unacceptable levels of benzene, acetaldehyde, or acetal. 74530-013-03 GSD Advanced Hand Sanitizer - 80% Alcohol Based - ( 1 Litter ( 33.2 OZ What to do: Stop using the identified product lots below. The recalls were issued on October 8 after undeclared impurities were found in the sanitizers. 79279-620-03 GSD Advanced Hand Sanitizer - Drugs.com 75339-751-04 The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. Recall of certain hand sanitizers that may pose health risks (Part 1 EO Hand Sanitizer Gel. CNN . [8/12/2020] FDA is warning consumers and health care professionals about certain hand sanitizer products, including those manufactured by Harmonic Nature S de RL de MI in Mexico, that are labeled to contain ethanol or isopropyl alcohol but have tested positive for 1-propanol contamination. 71120-117-02, 75821-001-01 79279-521-05 79279-610-02 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. 74046-006-07 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 For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. 74046-001-14 75821-002-03. Updated: Jul 13, 2020 / 11:49 AM PDT. Flavor Vapors, LLC, dba: Mob Liquid Labs FDA Expands List of Hand Sanitizers That Contain Toxic - Healthline Hand sanitizer is a great way to keep your hands clean while in public. 79279-620-05. 74046-001-07 Pleasant scent and safe for sensitive skin. Hand sanitizer recalled because it may cause methanol poisoning Health Canada recalling 19 hand sanitizers over health risks Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. The agency also included an additional denaturant formula in the temporary guidances. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. 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. HAN Archive - 00434 | Health Alert Network (HAN) - Centers for Disease FDA recommended the company recall on 9/14/2022; product voluntarily recalled on 9/17/2022; FDA issued a warning letter on 12/21/2022. 74530-011-03 GSD Disinfecting Sanitizing Wipes can be used for everyone. 74046-001-09 The newest recalled hand sanitizers are: The Food and Drug Administration has recalled more hand sanitizers with a new, deadly toxin bringing its growing "do not use" list to nearly 150 products. Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. 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. In most . 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. (China), Be Cleaner Be Healthier 75% Alcohol Wipes, One Drop Care Alcohol Disinfectant Wet Wipes, 75339-751-01 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): [1/19/2021] Today, FDA issued a guidance outlining the agencys policy for drug manufacturers and compounders to test alcohol or isopropyl alcohol for methanol contamination prior to using the alcohol to produce drugs, including hand sanitizer products. A company is recalling its hand sanitizers because they may contain impurities that could cause cancers through long-term exposure, according to a notice from the U.S. Food and Drug. Is purportedly made. 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. That chemical, according to the recall posted on the U.S. Food and Drug Administration's website, is . Learn more at poisonhelp.hrsa.gov/. The US Food and Drug Administration has expanded its warning about hand sanitizers to avoid, with the list now topping 100. To help limit the spread of COVID-19, wash your hands often with soap and water for at least 20 seconds. Is being recalled by the manufacturer or distributor. Grapefruit Extract, 74721-0010-1 Consumers who have been exposed to hand sanitizer containing 1-propanol and are experiencing symptoms should seek immediate care for treatment of toxic effects of 1-propanol poisoning. 74530-013-08, 74530-012-01 A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. 04:20. It was only four months ago that hand sanitizers became one of the hottest products to fly off the shelves around the world to help stave off the coronavirus. Individual Warp Wipes can use anywhere you need to clean hands or there's no water available. FDA expands hand sanitizer recall to at least 75 brands across the U.S. The agencys investigation of contaminated hand sanitizers is ongoing. (Florida), Salon Technologies International Sanitizing Hand Spray 80%. 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. GSD Hand Sanitizer, Hand Sanitizer, 33.8 Ounce Brand: GSD Hand Sanitizer 3 ratings Currently unavailable. 74721-0020-8 75821-001-03 74721-0001-3 75293-001-01, Coppercraft Distillery, LLC 74046-001-16 Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 FDA recommended the company recall on 9/14/2022; product voluntarily recalled lot 1166A on 9/17/2022; FDA issued a warning letter on 12/21/2022. The alcohol (ethanol) or IPA should be destroyed following guidelines for hazardous waste and the manufacturer or compounder should contact FDA regarding the test results and the alcohols source. 79279-421-07 Additionally, any repackers who distribute hand sanitizers and other ethanol or isopropyl alcohol-based drugs, should know who they are purchasing from and conduct the necessary due diligence to ensure the drugs they sell are safe for consumers. Grapefruit Extract, 74721-0001-1 Durisan voluntarily recalled its hand sanitizer product on March 24, 2021 and expanded their recall on April 16, 2021. New Hand Sanitizers May Pose Risks - Consumer Reports 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. 71120-612-07 74530-011-07 75293-001-04 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. The agency continues to add certain hand sanitizers to theimport alertto stop these products from legally entering the U.S. market and has issued warning letters to companies that violate federal law. In the letter, company asked the FDA to recall the contaminated batches of hand sanitizer, conduct an investigation of the products, and provide information to the public, among other things. Do not pour these products down the drain or flush them. Health Canada has recalled several hand sanitizers across the country over the last two years over concerns of potential health risks from using the products. 9 best hand sanitizers meeting CDC guidance - NBC News The pouch is resealable to ensure your wipes are always fresh. Product Number: 849AB/BA Product Name: Moisturizing Hand Sanitizer Issuing Date: April 22, 2020 Revision Date: None Revision Number: 0 Safety Data Sheet The supplier identified below generated this SDS using the UL SDS template. 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. The agency urges consumers not to use these subpotent products and has expanded its list to include subpotent hand sanitizers, in addition to hand sanitizers that are or may be contaminated with methanol. World Health Organization formula. The site is secure. Sun Wave Antiseptic Hand Sanitizer Alcohol Antiseptic 70% Enriched with Aloe Clean Scent. Methanol is not an acceptable ingredient for any drug and should not be used due to its toxic effects. 74530-013-04 Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality.
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