Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. Innovaciones Tecnologicas Concar, SA de CV 79279-620-05. (Mexico), SQ2SKIN Skin Care, Antiseptic Hand Sanitizer Foam (Benzalkonium Chloride 0.13%), 79279-420-01 Gsd Liquid Hand Sanitizer | Hand Sanitizers | Household | Shop The Exchange Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%. Infection can occur with use of the contaminated hand sanitizer by consumers or by health care professionals who may also transmit the contaminating bacteria to patients. 74721-0001-0 Contact your local waste management and recycling center for more information on hazardous waste disposal. The US Food and Drug Administration has expanded its warning about hand sanitizers to avoid, with the list now topping 100. FDA says not to use this hand sanitizer, may contain cancer - KRON4 GSD Advanced Hand Sanitizer - Gomer's of Kansas 80969-040-03 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). To date, the FDA's ongoing testing found methanol contamination in hand sanitizer products ranged from 1 percent to 80 percent. 74721-0002-6 Testing ethanol for methanol contamination is a quality standard set by the United States Pharmacopeia (USP) for alcohol used in pharmaceuticals (including hand sanitizers) and enforced by FDA pursuant to section 501(b) of the FD&C Act. 75821-001-02 Safety officials at the Food and Drug Administration are warning Americans that not all hand sanitizers are made equal,. Hand sanitizer recalls: FDA lists methanol hand sanitizers to avoid 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 01/05/2023, 74046-004-01 79279-620-01 75293-001-01, Coppercraft Distillery, LLC 74046-004-02 Consumer and health care professional safety is a top priority for FDA, and an important part of FDAs mission is to protect the public from harm, especially as we seek to help increase hand sanitizer supply. 74721-0020-9, 71120-112-01 That chemical, according to the recall posted on the U.S. Food and Drug Administration's website, is . If swallowed, call a poison control centre or seek medical help immediately. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. FDA updates on hand sanitizers consumers should not use Young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk. 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 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 methanol; product voluntarily recalled on 11/5/2022. Keep all hand sanitizers out of the reach of children. 74046-006-07 Some Hand Sanitizers Made During the Pandemic Have - Insider Alcohol Antiseptic 75% Topical Solution Hand Sanitizer. [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. What to do: Stop using the identified product lots below. 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. 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. 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. 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. GSD Advanced Hand Sanitizer - Drugs.com Consult your health care professional if you have used any of these products and have health concerns. It also reported that Target sold Born Basic Anti-Bac Hand Sanitizer, while Walmart sold Scent Theory at stores in 17 states. 74530-011-03 On Nov. 7, the FDA announced that Colorado-based Adam's Polishes, LLC had issued a voluntary recall for 20 lots of its Adam's Polishes Hand Sanitizer. Hideout Hand Sanitizer non-sterile solution Alcohol Antiseptic 80% Topical Solution. 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). The agency also reminds manufacturers of their ongoing obligation, in accordance with current good manufacturing practice (CGMP) requirements, to take all appropriate actions to prevent unsafe levels of methanol in drugs, including, but not limited to, purchasing alcohol or isopropyl alcohol from a reliable supplier, completing proper testing of alcohol or isopropyl alcohol, and reviewing finished product test methods to verify the testing distinguishes between the active ingredient and methanol. 74721-0010-8 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. 80969-010-06 Consumers should be aware that FDAs recommendation against using a distributors specific hand sanitizer product(s) manufactured by a particular manufacturer, as listed below, does not extend to: If a product on the list below does not identify the manufacturer on the label, consumers can contact the distributor whose name appears on the label to find out who manufactured the product. 75339-751-06, Dongguan Chunzhen Biological Technology Co., Ltd(China), GuangdongLongtaiIndustry 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 07/05/2022, GuangdongLongtaiIndustry 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 07/06/2022, Guangzhou Meiyichen Pharmaceutical Co. Ltd. (China), Guangzhou Minghui Cosmetics Co. Ltd.(China). FDA tested product; contains unacceptable levels of acetaldehyde and acetal; after FDA contacted the firm, firms testing identified benzene in another product. Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. ADVERTISEMENT. 7 and the U.S. Food & Drug Administration (FDA) posted the recall notice on the same date. The hand sanitizers include brands sold at Sam's Club and BJ's Wholesale Club. 71120-117-02, 75821-001-01 Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. 74530-013-08, 74530-012-01 Individuals with compromised immune systems are at increased risk. 74721-0001-8 The FDA announced a recall for a specific hand sanitizer. Add to Cart Overview GSD Liquid Hand Sanitizer kills more than 99.99% of the most common germs. When the FDA continues to issue recalls for the inclusion of potentially toxic ingredients (as of this release, the list of banned sanitizers has now surpassed 100), we all need a hand sanitizer . Medically Minded Hand Sanitizer Gel V-KLEAN DermX70 Hand Sanitizer (only includes 250mL, 500mL and 1000mL sized packages) V-KLEAN Hand Sanitizer Gel V-KLEAN Hand Sanitizer Gel. 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. 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. 74721-0001-7 08/11/2020. 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. 71120-112-06 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. 74046-001-07 The dangers of drinking any hand sanitizer under any conditions. 74046-001-13 The product, which contains 70% ethyl alcohol gel, comes in 8-ounce bottles and is intended to be . containers resembling food pouches labeled with childrens characters, including Barbie, Hot Wheels, Paw Patrol, Minions, JoJo Siwa Dreamer and Trolls World Tour, Hand sanitizer products packaged in containers resembling food pouches commonly used for childrens applesauce and other pureed foods that present increased risk of accidental ingestion by children; FDA recommended the distributor recall on 9/21/2020; this advisory does not extend to Smart Care products in other types of packaging; product voluntarily, Lite n Foamy Lemon Blossom Hand Sanitizer, Company tested product; contains microbial contamination; product voluntarily recalled on 7/1/2020 and on 3/29/2021; FDA issued a, Company tested product; contains microbial contamination; product voluntarily recalled on 7/1/2020; FDA issued a, Private D Capital Group Corp., Human Choice LLC and RediBag USA Astrum LLC, Bersih Antiseptic Alcohol 70% Topical Solution hand sanitizer, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/1/2020; added manufacturer to, SIREtizer Alcohol Antiseptic 80% Topical Solution Hand Sanitizer. 79279-520-08 GSD Hand Sanitizer And Disinfecting Wipes - FDA Approved Scentsational Soaps & Candles, Inc. issued a voluntary recall on the spray . Products labeled with harmful or poisonous ingredients, such as methanol. Dongguan Mingyi Medical Products, Co., Ltd. 74046-006-08 The FDA's list of dangerous hand sanitizers has now grown to - CNN 71120-112-08 Health Canada has issued a recall for 19 hand sanitizers because they may pose health risks. Unibeleza Industria E Comercio De COVID-19: List of hand sanitizers authorized by Health Canada - Canada.ca 74530-012-04 Do not use these hand sanitizers according to FDA - Washington Post The agency also included an additional denaturant formula in the temporary guidances. FDA recommended the company recall on 06/01/2022. Carcinogen found in hand sanitizer distributed by Yale 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. 79279-521-01 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. 74530-013-05 We will ensure that your family stays protected from dust. Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? 74721-0010-7 The United States Pharmacopeia (USP) revised the Alcohol (ethyl alcohol) monograph on September 1, 2020, and established a limit for methanol in alcohol of 200 parts per million (ppm).