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 79279-521-03 [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. 74530-013-07 Choose from Same Day Delivery, Drive Up or Order Pickup plus free shipping on orders $35+. Active ingredient. Conagra Brands, Inc. Unilever issued a recall for certain lot codes of its Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head) as well as TRESemm dry shampoo aerosol products after an internal investigation. 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. 74416-001-01 74046-006-09 75293-001-01, Coppercraft Distillery, LLC Regular price $19.99 Sale price $19.99 Regular price $19.99 Sale Sold out. 78378-888-02 . (Michigan). 79279-610-04 74721-0001-9 [7/31/2020] FDA continues to find issues with certain hand sanitizer products. 75821-002-02 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. 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. 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. , FDA Safety Recalls, Presence in Breast Milk. 74721-0010-4 The Suave lawsuit was filed after the release of a report by the independent, online pharmacy Valisure on November 3, which found dangerously high levels of benzene in deodorants and body sprays. Topical Solution. Children are particularly at risk with these products since ingesting only a small amount of hand sanitizer may be lethal in a young child. Purpose. 74721-0020-6 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. Uses. SkinSAFE has reviewed the ingredients of Suave Hand Sanitizer Spray, 10 fl oz (295 mL) and found it to be hypoallergenic and free of Fragrance, Gluten, Coconut, Nickel, Top Common Allergy Causing Preservatives, Lanolin, Paraben, Topical Antibiotic, MCI/MI, Soy, Propylene Glycol, Balsam of Peru, Oil, Irritant/Acid, Dye, and SLS. 74046-001-13 75821-002-03. 1,290. 74721-0002-6 70483-018-03, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality added manufacturer toimport alert to help stop their products from entering the U.S. on 04/03/2023, Guangzhou Cikang Biotechnology Co., Ltd. Nearly eight months prior to that recall, Valisure, a company that tests and checks the composition of different health-related products, had announced on March 24 that they had found benzene in. 75339-751-05 Benzene is a petrochemical often found in vehicle emissions. Dongguan Mingyi Medical Products, Co., Ltd. (China), 74046-001-01 71120-117-02, 75821-001-01 Additionally, any alcohol (ethanol) or IPA found to contain more than 630 ppm methanol does not fall within the policies described in the temporary guidances and may be considered evidence of substitution and/or contamination. Customers with questions regarding this recall may contact Family Dollar Customer Service at 844-636-7687 between 9 a.m. and 5 p.m. EST. Guangdong Theaoson Technology Co. Ltd. (China), Guangdong Theaoson Technology Co., Ltd. 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. 74046-001-20. 74046-001-17 When purchased online. McKesson Brand #53-28037-18. 74458-101-07 80969-040-04, PFA Stronghold Hand Sanitizer Warnings For external use only Flammable. PepsiCo Voluntarily Recalls Starbucks Frappuccino Vanilla Bottles 13.7 oz (foreign matter - glass) Sold at: Select Walmart Stores and Sam's Clubs. FDA tested product; contains unacceptable levels of methanol; FDA recommended the company recall on 3/22/2023; product voluntarily recalled on 3/27/2023. Benzene may cause certain types of cancer in humans. 80969-010-06 Shop the full suite of our hand sanitizers that will sanitize your hands from bacteria and germs. SUAVE HAND SANITIZER SPRAY - Ethyl Alcohol liquid Suave Hand Sanitizer Spray. 79279-520-07 79279-521-02 Flavor Vapors, LLC, dba: Mob Liquid Labs found to have inadequate concentrations of ethanol are NeoNatural, Medicare Alcohol Antiseptic Topical Solution, Datsen Hand Sanitizer and Alcohol. 75612-101-10 This hand sanitizer formula can be used on hands when soap and water are not available to clean hands and has no added fragrance. Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 3/22/2023; product voluntarily recalled on 3/27/2023. 74530-011-07 74530-013-06 The company said it has worked with its propellant suppliers to address the issue. (Wyoming), Snowy Range Blue alcohol antiseptic 80% topical solution, 75288-100-01 74458-101-03 MVP Sanitizing Services Spray Hand Sanitizer; Born Basic. 74530-012-08, Ningbo Pasco UnitedIndustry Co., Ltd.(China), Pasco Instant HandSanitizer Aloe &Moisturizers, Safe Cleaner Hand Sanitizer Gel Anti-Bac Hand Sanitizer 70% alcohol, Born Basic. ADVERTISEMENT. 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. 80969-010-07 79279-620-01 Suave hand sanitizer recall Question: is Suave hand sanitizer recalled? Anti-Bac Hand Sanitizer 65% Alcohol (Recalled in July 2020, the manufacturer has since corrected issues. FDA tested product; contains acetaldehyde and acetal contaminants. 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. 70483-018-01 [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. 74046-006-02 . 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. For more information, visit Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? 77492-006-25. 74530-013-03 Do not pour these products down the drain or flush them. Many products have tested positive for. More were added to the list last week. 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 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. Suave Essentials Antibacterial Hand Sanitizer Spray is 99.9% effective against many common germs and bacteria. Has been tested and is found to have microbial contamination. By Kelsie Sandoval. Health Canada has issued a recall for 19 hand sanitizers because they may pose health risks. 74721-0020-2 75821-001-04 Public health professionals have recommended frequent hand-washing to guard against covid-19. 74046-001-12 distilleries that manufacture their own hand sanitizer from alcohol they produce) and do not procure it from an outside source. Call 9-1-1 if the person is unconscious or has trouble breathing. (China), Be Cleaner Be Healthier 75% Alcohol Wipes, One Drop Care Alcohol Disinfectant Wet Wipes, 75339-751-01 74416-170-10, Nanomaterials Discovery Corporation 79279-421-07 $9 at Amazon $12 at Walmart. Instantly cleanse with the power of 80% alcohol. 75612-101-02 Sophora Extract 74046-001-03 74046-006-06 The recalled hand sanitizer list from the Food and Drug Administration (FDA) is growing. 71120-611-07 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. 79279-421-08 FDA recommended the company recall on 9/20/2021;product voluntarily recalled on 9/21/2021, SBL Brands LLC dba Global Sanitizers, LLC (Nevada), Hand sanitizer products packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA issued a, Scentsational Soaps and Candles Inc. (Florida), Scentsational Sanitizer Non-Sterile Solution Alcohol Antiseptic 70% Topical Solution, Company tested product; contains methanol, benzene and acetaldehyde; product voluntarily, Fresh Lemon Citron Frais Scented Hand Sanitizer, SS Black and White Collection and Photo Real Collection: Coconut Breeze; Eucalyptus & Mint; Lavender & Herbs; Lemon Zest; Tangerine & Guava, Sck Zeta Dis Ticaret Pazarlama Ltd. (Turkey), FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 1/20/2022; product voluntarily recalled on 1/28/2022. Recalls 2,581,816 lbs of Canned Meat and Poultry Vienna Sausages (packaging defect - damaged, leaking, spoilage) Health Canada has suspended the product licence for two of . Grapefruit Extract, 74721-0010-1 74046-004-03 Antiseptic. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. [10/28/2021] FDA is alerting health care professionals and consumers of artnaturals voluntaryrecall of limited batches of 8 oz bottles of Scent Free Hand Sanitizer. 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. 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. 78378-666-02 ALL PRODUCTS. Is made at a facility that did not respond to multiple FDA requests for information about the quality of their products and manufacturing process. Hand Moisturizers; Exfoliators & Scrubs; Body Treatments; Body Powder; Natural Bath & Body; Hand Soap; Hand Sanitizer; Scar & Stretch Mark Treatments; Bath Accessories; Body Sprays; Baby & Children's Bath; Bath & Body for Men; Shop Bath & Body; Sale on Bath & Body; Close menu 74416-170-03 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. 74530-011-04 ALL PRODUCTS. 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. Hand sanitizer product packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 6/17/2021, product recalled on 06/21/2021. 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. 70108-040-01 McKesson Brand #16-1068. Our alcohol-based hand sanitizer helps eliminate over 99.9% of many common harmful germs and bacteria. 74721-0001-3 FDA tested product; contains unacceptable levels of methanol, acetaldehyde and acetal; FDA recommended the company recall on 2/9/2023; product voluntarily recalled on 2/14/2023. FDA recommended the company recall on 06/01/2022. Is purportedly made at the same facility as products that have been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. Target Help Returns Track Orders Recalls . 74046-001-02 70483-018-02 75612-101-06 Contact your local waste management and recycling center for more information on hazardous waste disposal. Best Multipack: Suave . Masks . 74721-0010-9 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. Unilever in late March recalled two Suave 24-hour protection aerosol antiperspirants after an internal review found slightly elevated levels of benzene in some samples. 74458-101-06 Medline Plus . Handle in accordance with good industrial hygiene and safety practice. EIGHTYAID HAND SANITIZER ALCOHOL ANTISEPTIC 80% TOPICAL SOLUTION Why This Is Great . 79279-620-03 74046-004-09 Innovaciones Tecnologicas Concar, SA de CV $20.99. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. See list of stores. Hand Sanitizer Topical Solution, Alcohol Antiseptic 80%, 75293-001-02 78378-666-08, ProtectorPlus Hand Sanitizer, 75% alcohol, 78378-888-01 74610-008-08 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). 75612-101-37 75612-101-50, St. Augustine Distillery LLC 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 9/2/2022. 75612-101-13 Your product's name. 381. . 74530-013-08, 74530-012-01 78378-888-06 74046-006-08 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 4/24/2023. 75339-751-04 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. July 22, 2020, 10:12 AM PDT. 74046-001-06 The hand sanitizer gel formula can be used on hands when soap and water are not available. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. 74458-101-04 Florance Morris Body Care Antispetic Hand Sanitizer, FDA tested product; contains methanol; FDA recommended the company recall on 8/13/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; added manufacturer to, FDA tested product; contains methanol; FDA recommended the company recall on 7/1/2020; added manufacturer to, M Hand Sanitizer Alcohol Antiseptic topical solution 80% Topical Solution Hand Sanitizer, FDA tested product; contains methanol; FDA recommended the company recall on 8/20/2020; added manufacturer to, Hand Sanitizer Alcohol Antiseptic topical solution 80%, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 8/20/2020; added manufacturer to, Jalisco Paper Inc. SOFT HANDS Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution, Foshan Meixin Biotechnology Co., Ltd.; formerly, Meixin Beauty & Health Care Products Co., Ltd (China), Macys Antibacterial Hand Sanitizer Gel (75% ethyl alcohol). 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. Learn more at poisonhelp.hrsa.gov/. Drivergent Hand Sanitizer, Alcohol Antiseptic 80% Topical Solution, Antiseptic Hand Rub, Non-Sterile Solution. Consumers who have products on thelist of hand sanitizerswith potential contamination should immediately stop using the product and dispose of it, ideally in ahazardous waste container. Voluntary Dry Shampoo Recall; Voluntary Aerosol Antiperspirants Recall . Unilever recalled the following Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head) and Tresemm dry shampoo . 55028-004-01 74416-002-01 Alcohol-based hand sanitizers that are contaminated with methanol are subject to adulteration charges under the FD&C Act. Alcohol Free Disinfectant, Safe Cleaner Plus The recalls were issued on October 8 after undeclared impurities were found in the sanitizers. In a convenient 10 oz bottle with an easy-to-use spray top our Suave . This dry shampoo recall was at least the sixth recall this year involving benzene, according to the F.D.A.'s data. Methanol is not an acceptableingredient for hand sanitizers and must not be used due to its toxic effects. Hand sanitizers that are sold or offered for sale with false and misleading, unproven claims that they can prevent the spread of viruses such as COVID-19, including claims that they can provide prolonged protection (e.g., for up to 24-hours). 71120-112-10 Foshan Meixin Biotechnology Co., Ltd.; formerly, Meixin Beauty & Health Care Products Co., Ltd Suave 24-Hour Protection Aerosol Antiperspirant . . 79279-420-02 It has 62 percent ethyl . 75612-101-25 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. Drug Facts. Hand Sanitizers Use our Suave Hand Sanitizers when soap and water are not available to help eliminate over 99.9% of many common harmful germs and bacteria. Denaturing alcohol in hand sanitizers is critical to deter children from unintentional ingestion. Learn more about this product. 80969-020-03 74721-0010-2 Recall roundup: Disney-branded hand sanitizers, Suave antiperspirants, smoke alarms & rattles recalled Testing detected toxic chemicals in hand sanitizers, antiperspirants Best for travel: Touchland Power Mist. 74721-0002-3 Animal studies indicate that the central nervous system depressant effects of 1-propanol are 2 to 4 times as potent as alcohol (ethanol). 78378-888-08. MVP Sanitizing Services Spray Hand Sanitizer: 76947-198-20 76947-198-21 76947-199-21: . The agency also included an additional denaturant formula in the temporary guidances. 4 oz. Travel hand sanitizer in a convenient 8 oz. Shop Target for hand sanitizer refill you will love at great low prices. Safeguard against germs. Best sanitizer wipes: Oars + Alps Antibacterial Aloe Wipes. The temporary guidances have also been updated to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities. FDA recommended the company recall on 06/01/2022. Here are the best hand sanitizers: Best Scent: Megababe Squeaky Clean Hand Sanitizer. 79279-521-01 (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 4/24/2023, Natuurs Advance Hand Sanitizer Alcohol Antiseptic 80%. 75612-101-04 79279-620-04 Suave Hand Sanitizer kills 99.9% of germs. 79279-520-08 74610-008-16 74046-001-10 Hand Sanitizer; Hand Sanitizer Wipes; Search Log in Cart. 74663-002-55 The FDA has listed 255 different hand sanitizers, mostly produced and distributed in Mexico, that. 74721-0002-1 Hand Sanitizer; All Hand Products; All Body Products; Deodorant Products. 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. Your product's name. 79279-421-10 Skip to main content. The Food and Drug Administration has updated its recall list to include 149 different hand sanitizers due to failing standards on randomized tests. 74046-001-14 Ingredients. 06/23/2021. 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 import alert to help stop their products from entering the U.S. on 09/09/2022. Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. 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 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. 75293-001-03 78378-888-05 Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. 79279-521-05 Best spray: Bare Hands Hand Sanitizer. Mint Oil 74721-0020-8 Dr. Bronner's Organic Hand Sanitizer - Lavender. 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. Acure's five-ounce bottle includes moisturizing aloe vera and 70% ethanol to fight both dryness and germs. 74046-001-18 74416-170-02 Durisan voluntarily recalled its hand sanitizer product on March 24, 2021 and expanded their recall on April 16, 2021.. 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. 74610-008-01 79279-420-03 74046-006-07
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