71120-112-05 79279-420-04 Acetal can irritate the upper respiratory tract, eyes, and skin. 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 1/24/2023. The US Food and Drug Administration has expanded its warning about hand sanitizers to avoid, with the list now topping 100. 79279-520-07 74046-001-05 GSD Liquid Hand Sanitizer Item: #2353632 4.2 (14) $1.97 Save 15% with MILITARY STAR Plans Size: 33.8 oz. No rinse needed, usable anywhere without water. There's a nationwide spray hand sanitizer recall on 11 products that were sold at Ulta, TJ Maxx, and Marshalls stores. 74046-001-15 $8.19. The product, which contains 70% ethyl alcohol gel, comes in 8-ounce bottles and is intended to be . 74530-011-08, 74530-013-01 Flavor Vapors, LLC, dba: Mob Liquid Labs 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. Canada's health agency has added three more hand sanitizer products to its growing list of 48 recalled items which began in the spring of 2021. 75339-751-05 Suite #166 Las Vegas, NV 89139";FDArecommended the company recallon11/3/2021;product voluntarilyrecalledon11/4/2021, Medically Minded Antimicrobial Hand Sanitizer Gel with Vitamin E and Moisturizer, SBL Brands LLC dba Global Sanitizers LLC(Nevada), FDA tested product; contains methanol; FDA has been unable to determine the manufacturer to recommend a recall; FDA recommended the distributor recall on 5/6/2021; product voluntarily, Medically Minded Hand Sanitizer Gel Anitmicrobial Formula, Products possibly made at the same facility that produced methanol contaminated product; FDA has been unable to determine the manufacturer to recommend a recall; FDA recommended the distributor recall on 5/6/2021; product voluntarily, Medically Minded Hand Sanitizer Gel Antimicrobial Formula with Vitamin E and Moisturizer, Product labeled to contain methanol; FDA recommended the company recall on 8/7/2020; product voluntarily recalled on 8/14/2020, WelburnGlobal SociedadAnonima(Guatemala), Product manufactured at a facility that did not respond to multiple FDA requests for recordsrelated to drug manufacturing and product qualityeven after receiving a warning letter. 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. The newest recalled hand sanitizers are: Additionally, FDA reminds consumers that no drugs, including hand sanitizers, are approved to prevent the spread of COVID-19. 75821-001-03 The agency continues to add certain hand sanitizers to import alert to stop these products from legally entering the U.S. market. FDA tested product; contains acetaldehyde and acetal contaminants. List of antiseptic or antibacterial skin cleansers or hand sanitizers meeting Health Canada's requirements for safety, effectiveness and quality, for use against coronavirus (COVID-19). 75339-751-02 75821-002-01 74721-0001-0 Proton Armor Antimicrobial Alcohol-Free Foaming Hand Sanitizer. 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 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. 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. The ITECH 361 recall is for 18,940 bottles of All Clean hand sanitizer sold in one-liter bottles with UPC Code 628055370130. Add to Cart Overview GSD Liquid Hand Sanitizer kills more than 99.99% of the most common germs. 74530-013-04 74530-012-03 74721-0002-7 Maridav/Shutterstock. 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. That chemical, according to the recall posted on the U.S. Food and Drug Administration's website, is . 79279-521-02 74721-0010-4 74721-0002-1 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. April 30, 2021 -- Nearly a dozen scented hand sanitizer sprays sold at Ulta, TJ Maxx, and Marshalls stores nationwide are being recalled because they may be contaminated with methanol, a. 75821-001-04 Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. 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. Specifications Value of Product Features Most Helpful Favorable Review Good stuff ! The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. Ingesting 1-propanol can cause central nervous system (CNS) depression, which can result in death. Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%. GSD Advanced Hand Sanitizer Dosage form: gel, metered Ingredients: ALCOHOL 0.7mL in 1mL Labeler: JoCo Sales & Marketing, Inc. NDC code: 77784-000 Medically reviewed by Drugs.com. Safety officials at the Food and Drug Administration are warning Americans that not all hand sanitizers are made equal,. Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. 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. It also reported that Target sold Born Basic Anti-Bac Hand Sanitizer, while Walmart sold Scent Theory at stores in 17 states. FDA will consider revising the list as appropriate. Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. 79279-610-01 Keep all hand sanitizers out of the reach of children. 74721-0001-2 (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 80969-020-03 74530-013-07 Updated: Nov 9, 2022 / 01:55 PM EST. Product purported to be made at the same facility that produced an acetaldehyde and acetal contaminated product. 75293-001-04 Animal studies indicate that the central nervous system depressant effects of 1-propanol are 2 to 4 times as potent as alcohol (ethanol). FDA tested product; contains methanol; product voluntarily recalled on 11/5/2022. 74046-001-13 USPs revision bulletin for alcohol and dehydrated alcohol monographs outlines this testing requirement, official as of September 1, 2020, which FDA requested to protect health care providers and consumers from using dangerous hand sanitizer products. 79279-620-03 The agency tweeted on Monday about the two latest recalls. 74046-004-05 Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. The Food and Drug Administration has expanded the list of hand sanitizers some sold at Walmart, Costco and other national chains being recalled to at least 75 recently, saying toxic. 74046-004-10, Benzalkonium Chloride Instant Hand Sanitizer, 74046-006-01 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; FDA recommended the company recall on 09/27/2022; product voluntarily recalled on 9/27/2022. 71120-112-08 74721-0020-9, 71120-112-01 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. (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): [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. Add to cart. 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. 79279-521-03 79279-421-07 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. 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. 79279-620-05. 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.