The agency is aware of adults and children ingesting hand sanitizer products contaminated with methanol that has led to recent adverse events including blindness, hospitalizations and death. 55028-009-01 FILTER BY: Clear all Filter by: Most Popular Sort by: Essentials Pink Honeysuckle Hand Sanitizer Buy Now Essentials Ocean Breeze Hand Sanitizer Buy Now Unscented Hand Sanitizer Buy Now Top 78378-666-07 55028-005-01 The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. 74046-001-07 77492-006-25. Find many great new & used options and get the best deals for Suave HUGE 10 Oz Bottle of Hand Sanitizer Spray at the best online prices at eBay! Denaturing alcohol in hand sanitizers is critical to deter children from unintentional ingestion. The site is secure. Methanol, or wood alcohol, is a substance that can be toxic when absorbed through the skin or ingested and can be life-threatening when ingested. Antiseptic. 79279-620-02 The agency also included an additional denaturant formula in the temporary guidances. 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. Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. Mint Oil 79279-421-09 Keep your skin soft and supple with hand and body lotion from Suave. Home; Hand Sanitizer; Hand Sanitizer Wipes; Featured collection. 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). 79279-610-03 Learn more at poisonhelp.hrsa.gov/. 74046-001-10 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. 74530-011-02 . 70% Alcohol Cleansing Gel Say Goodbye to Germs. The Honest Company Hand Sanitizer Spray - Grapefruit Grove - 2 fl oz. Dongguan Mingyi Medical Products, Co., Ltd. (China), 74046-001-01 Hand Sanitizer; All Hand Products; All Body Products; Deodorant Products. Hand sanitizers. 75612-101-05 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. But trace . 74046-004-09 SUAVE HAND SANITIZER SPRAY - Ethyl Alcohol liquid Suave Hand Sanitizer Spray. 75612-101-06 product voluntarilyrecalledon 11/30/2021, Product labeled to contain methanol; FDA recommended the company recall on 12/6/2021; product voluntarily recalled on 12/6/2021, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality even after receiving a warning letter. Medline Plus . Credit: Amazon. Your product's name. Mint Oil The test method for methanol described in the USP Alcohol Monograph can also be used to test for methanol contamination in isopropyl alcohol. [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. Alcohol-based hand sanitizers that are contaminated with methanol are subject to adulteration charges under the FD&C Act. 74046-001-08 70108-040-01 71120-112-06 Related Resources. 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. Feb to Apr 2021. Instantly cleanse with the power of 80% alcohol. Animal studies indicate that the central nervous system depressant effects of 1-propanol are 2 to 4 times as potent as alcohol (ethanol). Hello Bello Hand Sanitizer Spray Alternate Brand Names: SiO2 Innovation Labs Hand Sanitizer Spray; Carry Clean Hand Sanitizer Spray; DEFCON 1 Hand Sanitizer Spray; McCaughey Consumer Products Hand Sanitizer Spray: Not properly labelled (improper directions for use in children); sold without proper testing: Unconditional Love Canada, Inc . Suave Hand Sanitizer Spray - 10 FZ. Best pocket-size hand sanitizer Noshinku Pocket Hand-Sanitizer Discovery Pack - Eucalyptus, Lavendula, Bergamot $26 Buy at Noshinku Noshinku Pocket Hand-Sanitizer Discovery Pack - Eucalyptus. FDA tested product; contains unacceptable levels of acetaldehyde and acetal; after FDA contacted the firm, firms testing identified benzene in another product. Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. 74721-0002-7 74046-004-08 PepsiCo Voluntarily Recalls Starbucks Frappuccino Vanilla Bottles 13.7 oz (foreign matter - glass) Sold at: Select Walmart Stores and Sam's Clubs. 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). Give It A Rub. 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. In June, the FDA warned consumers not to use nine kinds of hand sanitizers because they may contain methanol, and added to the list in early July. The Food and Drug Administration has expanded the list of hand sanitizers some sold at Walmart, Costco and other national chains being . 79279-521-01 The recalled hand sanitizer list from the Food and Drug Administration (FDA) is growing. Recall roundup: Disney-branded hand sanitizers, Suave antiperspirants, smoke alarms & rattles recalled Testing detected toxic chemicals in hand sanitizers, antiperspirants 79867-002-02 Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? Uses . 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 [10/4/2021]FDA has tested certain artnaturals scent free hand sanitizer labeled with DIST. 74530-012-04 Suave Hand Sanitizer kills 99.9% of germs. Learn more at poisonhelp.hrsa.gov/. Methanol is not an acceptableingredient for hand sanitizers and must not be used due to its toxic effects. If soap and water are not readily available, the Centers for Disease Control and Prevention. 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. The agency will provide additional information as it becomes available. 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. 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. 78378-666-05 74046-006-10. FDA has updated our guidances to provide clarification that companies test each lot of the active ingredient (ethanol or isopropyl alcohol (IPA)) for methanol if the ethanol or IPA is obtained from another source. 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. For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. 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). 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. 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. 74458-101-03 79279-520-06 74416-170-02 Generally, all manufacturers and compounders that produce drugs containing ethanol must conduct the limit test for methanol, using the test method that appears in the USP Alcohol monograph. 79279-610-02 55028-003-01 74046-004-02 Oct 9 2021, 10:23 am. 71120-112-10 FDA is not aware of any adverse events related to Durisans hand sanitizer products. 78378-666-02 74046-001-09 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). Hand Sanitizer with Aloe McKesson 4 oz. 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. For more information, visit Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. Innovaciones Tecnologicas Concar, SA de CV This testing method can be used to help assure hand sanitizers contain the correct ingredients and do not contain harmful levels of impurities. McKesson Brand #53-28037-18. 78378-888-07 75821-002-02 Product Description Suave Hand Sanitizer kills 99.9 percent of germs. Unit price / per . 74530-012-06 75612-101-37 75612-101-50, St. Augustine Distillery LLC 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. Hand Sanitizer Industrial and Hospital Grade, FDA tested product; ethyl alcohol level was subpotent; added to, Guangzhou Youxing Cosmetics Co. Ltd.(China), V&W Advance Hand Sanitizer Refreshing Gel, Guangzhou Youxing Cosmetics Co. Ltd. (China), V&W Moisturizing Refreshing Spray Sanitizer [isopropyl alc. 80969-008-01, 80969-010-01 75339-751-03 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. Suave hand sanitizer recall Question: is Suave hand sanitizer recalled? 74530-011-06 . 70108-039-01 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. 71120-612-07 74610-008-01 (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 Sophora Extract Acetal can irritate the upper respiratory tract, eyes, and skin. , FDA Safety Recalls, Presence in Breast Milk. 55028-004-01 LEARN MORE. 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 MSDS NUMBER: 4053 CORPORATE ADDRESS: Unilever 700 Sylvan Avenue Englewood Cliffs, NJ 07632 PHONE #: 800-782-8301 Monday thru Friday (8:30 AM - 6:00 PM EST) EMERGENCY #: 800-745-9269 (24 Hours) POISON CONTROL #: 800-949-7866 (24 Hours) CHEMTREC #: 800-424-9300 (24 Hours, Transportation Emergencies) 79279-421-06 Public health professionals have recommended frequent hand-washing to guard against covid-19. 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. 79279-610-01 ALL PRODUCTS. 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. PRODUCTS. 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). 74530-013-06 74046-006-08 74530-013-05 74530-013-08, 74530-012-01 74530-013-03 In a convenient 10 oz bottle, with . 74416-170-10, Nanomaterials Discovery Corporation 74721-0001-5 4.6 out of 5 stars with 381 ratings. Young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk. FDA recommended the company recall all drug products on 12/12/2022; FDA issued a warning letter on 02/15/2023. The new additions contain a substance. 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. Jarmans Midwest Cleaning Systems, Inc. (South Dakota), Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution, 74663-001-04 It has 62 percent ethyl . 79279-421-07 74046-001-12 (118 mL) Helps reduce harmful bacteria on skin. 4 oz. 74416-170-07 The .gov means its official.Federal government websites often end in .gov or .mil. 75612-101-10 74046-001-04 FDA tested product; contains unacceptable levels of methanol; FDA recommended the company recall on 3/22/2023; product voluntarily recalled on 3/27/2023. 74046-004-03 Alcohol Free Disinfectant, Safe Cleaner Plus Health Canada issued a mass hair product recall over the detection of the cancer-causing chemical benzene. Ethyl Alcohol Gel Pump Bottle. 74530-015-06, 74530-011-01 This lightweight hand sanitizer spray dries quickly and leaves hands feeling fresh and clean. 79279-521-04 Drivergent Hand Sanitizer, 80% Alcohol Antiseptic Topical Hand Rub, Non-Sterile, 1 Quart, 32 FL OZ (0.95 L), Drivergent Hand Sanitizer 70% Alcohol Antiseptic Topical Hand Rub, Non-Sterile Solution, Gel, 8 FL OZ (250 ml), Drivergent Hand Sanitizer, 70% Alcohol Antiseptic Topical 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. 74721-0001-4 (Michigan). 74046-001-03 74416-170-08 Anti-Bac Hand Sanitizer 70% alcohol, Born Basic. Restaurant Supplies Hand Sanitizer, FDA tested product; ethyl alcohol level was subpotent; product was manufactured at the same facility that produced methanol contaminated product; FDA recommended the company recall on 8/20/2020; added manufacturer to, Yacana Alcohol Antiseptic 70% Topical Solution, FDA tested product; contains methanol; FDA recommended the company recall on 8/12/2020; product voluntarily, Yacana Isopropyl Alcohol Antiseptic 70% Topical Solution, FDA tested product; isopropyl alcohol level was subpotent; FDA recommended the company recall on 8/12/2020; product voluntarily, Yacana Clase Mundial Isopropyl Alcohol Antiseptic 70% Topical Solution or Gel, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 8/12/2020; product voluntarily, Guangdong Kemei Pharmaceutical Technology Co. Ltd. (China), FDA tested product; contains methanol; product voluntarily recalled by, Guangdong Kemei Pharmaceutical Technology Co. Ltd, KLEAN KARE Hand Sanitizer Industrial and Hospital Grade, Essentials, M.D. FDA tested product; contains methanol; product voluntarily recalled on 11/5/2022. 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. 74416-004-01, 74416-170-01 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 1/24/2023. Suave Essentials Antibacterial Hand Sanitizer Spray is 99.9% effective against many common germs and bacteria. 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. 74721-0002-6 Hideout Hand Sanitizer non-sterile solution Alcohol Antiseptic 80% Topical Solution. ADVERTISEMENT. FDA tested product; contains acetaldehyde and acetal contaminants. 74721-0020-5 Our alcohol-based hand sanitizer helps eliminate over 99.9% of many common harmful germs and bacteria. 74721-0020-8 80969-007-01 All . headerOutFocus. FDA will consider revising the list as appropriate. 74721-0010-2 Health Canada has issued a recall for 19 hand sanitizers because they may pose health risks. 79279-521-02 Browse the wide selection of lotions, hand creams, and more to prevent dryness. 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. 79279-420-02 FDA tested product; contains unacceptable levels of 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. 74530-011-07 06/23/2021. 74530-013-07 70483-018-01 Is being recalled by the manufacturer or distributor. 74046-001-16 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. 74721-0010-5 These are the best hand sanitizers: Best overall: Purell Advanced Hand Sanitizer. The recalls were issued on October 8 after undeclared impurities were found in the sanitizers. Keep away from fire or flame Avoid contact with eyes, in case of contact, rinse eyes thoroughly with water immediately. 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. [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. 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. 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. Safeguard's hand sanitizer kills 99.9% of bacteria*. Drug Safety and Availability, Recalls, Market Withdrawals and Safety Alerts, Information about Nitrosamine Impurities in Medications, Food and Drug Administration Overdose Prevention Framework, Medication Errors Related to CDER-Regulated Drug Products, Postmarket Drug Safety Information for Patients and Providers, Risk Evaluation and Mitigation Strategies | REMS, Multistate outbreak of fungal meningitis and other infections, FDA updates on hand sanitizers consumers should not use, 10/12/2021: FDA In Brief: FDA Withdrawing Temporary Guidances for Alcohol-Based Hand Sanitizers, 10/4/2021: UPDATE - FDA advises consumers not to use certain artnaturals hand sanitizers, local waste management and recycling center, Centers for Disease Control and Prevention, 3/25/2021: UPDATE - FDA warns consumers not to use Durisan Antimicrobial Solutions recalled Hand Sanitizer Alcohol-Free due to microbial contamination, 1/26/2021: PRESS RELEASE - Coronavirus (COVID-19) Update: FDA Takes Action to Place All Alcohol-Based Hand Sanitizers from Mexico on Import Alert to Help Prevent Entry of Violative and Potentially Dangerous Products into U.S., Protect U.S. Consumers, 1/19/2021: UPDATE - FDA Provides Policy for Testing of Alcohol (Ethanol) and Isopropyl Alcohol for Methanol, Including During COVID-19 Public Health Emergency, 8/27/2020 PRESS RELEASE - COVID-19 Update: FDA Warns Consumers About Hand Sanitizer Packaged in Food and Drink Containers, 8/24/2020: UPDATE FDA provides testing method to assess the quality of hand sanitizer products for impurities, 8/12/2020: UPDATE - FDA expands hand sanitizer warnings to include 1-propanol contamination, 8/7/2020: UPDATE - FDA Includes Methanol Testing in Temporary Policies for Alcohol-Based Hand Sanitizers, 7/31/2020: UPDATE - FDA continues to find issues with certain hand sanitizer products, 7/27/2020 PRESS RELEASE - Coronavirus (COVID-19) Update: FDA Reiterates Warning About Dangerous Alcohol-Based Hand Sanitizers Containing Methanol, Takes Additional Action to Address Concerning Products, 7/2/2020: UPDATE- FDA warns consumers of risk of methanol contamination in certain hand sanitizers, 7/2/2020 PRESS RELEASE - FDA Takes Action to Warn, Protect Consumers from Dangerous Alcohol-Based Hand Sanitizers Containing Methanol, 6/19/2020 ALERT - FDA advises consumers not to use hand sanitizer products manufactured by Eskbiochem. 74721-0001-0 Drivergent Hand Sanitizer, Alcohol Antiseptic 80% Topical Solution, Antiseptic Hand Rub, Non-Sterile Solution. Warnings For external use only Flammable. FDA issued, Alcohol Isopropilico Hand Sanitizer Limar, Hand sanitizer product packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 6/16/2021; added manufacturer to import alert to help stop their products from entering the U.S. on 6/30/2021;product, Blumen Clear Advanced Hand Sanitizer with 70% Alcohol with Glycerin and Aloe, FDA tested product; contains methanol; FDA recommended the company recall on 7/6/2020; added manufacturer to, BLUMEN Advanced Instant Hand Sanitizer Clear with 70% Ethyl Alcohol with Glycerin & Vitamin E, FDA tested product; contains methanol; FDA recommended the company recall on 7/6/2020; product voluntarily, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/6/2020; added manufacturer to, MODESA Instant Hand Sanitizer Moisturizers and Vitamin E, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/6/2020; product voluntarily, BLUMEN Advanced Instant Hand Sanitizer Lavender, BLUMEN Clear LEAR Advanced Hand Sanitizer, BLUMEN Clear Advanced Instant Hand Sanitizer, BLUMEN Clear Advanced Instant Hand Sanitizer Aloe, BLUMEN Clear Advanced Instant Hand Sanitizer Lavender, BLUMEN Aloe Advanced Hand Sanitizer, with 70 Alcohol, Blumen Advanced Hand Sanitizer Lavender, with 70% alcohol, Blumen Advanced Hand Sanitizer Aloe, with 70% alcohol, Blumen Antibacterial Fresh Citrus Hand Sanitizer, Hello Kitty Hand Sanitizer; this is not an official Sanrio licensed product, Assured Instant Hand Sanitizer (Vitamin E and Aloe), Assured Instant Hand Sanitizer (Aloe and Moisturizers), Assured Instant Hand Sanitizer Vitamin E and Aloe, Assured Instant Hand Sanitizer Aloe and Moisturizers, BLUMEN Instant Hand Sanitizer Fragrance Free, FDA tested product; contains methanol; FDA recommended the company recall on 7/2/2020; added manufacturer to, bio aaa Advance Hand Sanitizer 480 mL bottles, Product purported to made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 8/26/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/2/2020; added manufacturer to, FDA tested product; contains methanol; FDA recommended a recall on 7/27/2020; product voluntarily, NuuxSan Instant Antibacterial Hand Sanitizer, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/27/2020; product voluntarily, Assured Instant Antiseptic Hand Sanitizer with Aloe and Moisturizers, Assured Instant Antiseptic Hand Sanitizer with Vitamin E and Aloe, Modesa Instant Antiseptic Hand Sanitizer with Moisturizers and Aloe Vera, Modesa Instant Antiseptic Hand Sanitizer with Moisturizers and Vitamin E, Asesores en Mantenimiento Hidrulico e Industrial SA de CV (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 8/31/2020; added manufacturer to, Asesores en Mantenimiento Hidrulico e Industrial, SA de CV (Mexico), Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 08/31/2020; added manufacturer to, FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 8/5/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 8/5/2020; added manufacturer to, DermX70 Hand Sanitizer (only includes 250mL, 500mL and 1000mL sized packages), SBL Brands LLC dba Global Sanitizers LLC (Nevada) LLC dba Global Sanitizers LLC (Nevada), Protz Real Protection Antibacterial Hand Sanitizer, FDA tested product; contains methanol; FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product, Product purported to be made at the same facility that produced methanol contaminated product;FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product, AltaioHand Sanitizing Wipes (80% Ethanol), Product purported to be made at the same facility that produced methanol contaminated product;FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product;addedmanufacturerto, AltaioHand Sanitizing Wipes (70% Ethanol), Naturia Professional Green Hand Sanitizer, Essentials by Urban Secrets Hand Sanitizer, Essentials by Urban Secrets Advanced Hand Sanitizer, Botanicals Internacional SA de CV (Mexico), Alcohol Antiseptic 80% topical solution hand sanitizer, Product purported to be made at the same facility that produced methanol contaminated product; FDA has no evidence this product is in the U.S. market; added manufacturer to, Inatek Hand Sanitizer Non-Sterile Solution 70% of Alcohol, FDA tested product; contains methanol; FDA has no evidence this product is in the U.S. market; added manufacturer to, Total Pure Alcohol Based Hand Sanitizer Gel, Bottle Tree Beverage, LLC, dba: Cathead Distillery (Mississippi).

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