Recall of certain hand sanitizers that may pose health risks (Part 1 Free shipping for many products! You'll Like It. 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. This easy-to-use spray has the added calming effect of a lavender scent. 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. Problems with Hand Sanitizer Formulation, Labels Highlighted in Study Here are the best hand sanitizers: Best Scent: Megababe Squeaky Clean Hand Sanitizer. Choose from Same Day Delivery, Drive Up or Order Pickup plus free shipping on orders $35+. 74046-001-08 79279-421-09 74721-0001-3 Individuals with compromised immune systems are at increased risk. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. 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. 74046-006-03 74530-012-06 Do not pour these products down the drain or flush them. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 This alcohol-based hand sanitizer helps eliminate over 99.9% of many common harmful germs and bacteria. (China). The four hand sanitizers the F.D.A. 75821-001-02 74663-001-12 Recalls 2,581,816 lbs of Canned Meat and Poultry Vienna Sausages (packaging defect - damaged, leaking, spoilage) Your product's name. 74530-012-05 Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. 74530-012-04 55028-004-01 FDA tested product; contains unacceptable levels of methanol; FDA recommended the company recall on 3/22/2023; product voluntarily recalled on 3/27/2023. Health Canada issued a mass hair product recall over the detection of the cancer-causing chemical benzene. 71120-112-11 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. Best gel: Palmpalm Hand Sanitizer Gel. 255 FDA-Recalled Hand Sanitizers to Beware of as COVID-19 - Newsweek 70108-040-01 Suave Hand Sanitizer Spray - 10 FZ - Safeway 75821-002-02 FRESH CLEAN SCENT. NOW PLAYING. Unilever is recalling all lots of the products below with an expiration date through September 2023. headerOutFocus. Superfy - Superfyshop 381. . Acetal can irritate the upper respiratory tract, eyes, and skin. The Honest Company. 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. 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. 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). FDA is not aware of any adverse events related to Durisans hand sanitizer products. Suave Pink Honeysuckle Hand Sanitizer with Aloe and Moisturizers helps you stay clean and safe while leaving skin feeling and smelling fresh. Shop the full suite of our hand sanitizers that will sanitize your hands from bacteria and germs. Hand sanitizer recalls: FDA lists sanitizers to avoid due to methanol Need help now? Ethyl Alcohol Gel Pump Bottle. 75339-751-02 (China), Smart Care Hand Sanitizer Aloe Vera & Vitamin E, 70108-038-01 Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. 75612-101-13 79279-610-05 Uses. The new additions contain a substance. 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. 75612-101-04 Products labeled with harmful or poisonous ingredients, such as methanol. 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. 74610-008-08 80969-020-03 74416-170-03 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. Disney hand sanitizer recall: Methanol, benzene in Baby Yoda, Mickey Animal studies indicate that the central nervous system depressant effects of 1-propanol are 2 to 4 times as potent as alcohol (ethanol). , FDA Safety Recalls, Presence in Breast Milk. The agency will provide additional information as it becomes available. 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 75288-100-02 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. 74046-001-19 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): [3/25/2021] FDA is warning consumers and health care professionals not to use Durisan Antimicrobial Solutions Hand Sanitizer manufactured by Sanit Technologies LLC doing business as Durisan in Sarasota, Florida, due to microbial contamination. 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). 74721-0020-8 Antibacterial Hand Sanitizer with Moisturize, Guangdong Theaoson Technology Co. Ltd. (China), Guangdong Theaoson Technology Co., Ltd. (China), Guangdong JunBao Industry Co. Ltd. (China), JPR Medical Disinfecting Wipes (75% alcohol), Guangdong JunBao Industry Co., Ltd. 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. Contact your local waste management and recycling center for more information on hazardous waste disposal. Hand Sanitizers - McKesson Medical-Surgical 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. 74530-013-08, 74530-012-01 Hand Sanitizer Refill : Target 79279-520-07 Suave Hand Sanitizer Kills 99.9% of Germs Alcohol Based Antibacterial Shop Hand Sanitizer and other Bath & Body products at Walgreens. PepsiCo Voluntarily Recalls Starbucks Frappuccino Vanilla Bottles 13.7 oz (foreign matter - glass) Sold at: Select Walmart Stores and Sam's Clubs. Our alcohol-based hand sanitizer helps eliminate over 99.9% of many common harmful germs and bacteria. 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. 80969-007-01 74721-0002-7 Guangzhou Yilong Cosmetics Co., Ltd. 75612-101-03 Hand Sanitizer | Suave The site is secure. Suave hand sanitizer recall Question: is Suave hand sanitizer recalled? All . 74416-170-05 Skin or eye exposure to 1-propanol can result in irritation, and rare cases of allergic skin reactions have been reported. Anti-Bac Hand Sanitizer 65% Alcohol (Recalled in July 2020, the manufacturer has since corrected issues. (Michigan). 74416-170-10, Nanomaterials Discovery Corporation 71120-117-02, 75821-001-01 FDA updates on hand sanitizers consumers should not use 74046-004-09 74046-004-04 Sun Wave Antiseptic Hand Sanitizer Alcohol Antiseptic 70% Enriched with Aloe Clean Scent. 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. [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. Give It A Rub. 74721-0002-4 74721-0001-8 Product Description Suave Hand Sanitizer kills 99.9 percent of germs. 74721-0001-7 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. FDA will consider revising the list as appropriate. 10 Best Hand Sanitizers 2023 | The Strategist 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. 79279-620-05. Unibeleza Industria E Comercio De Suave HUGE 10 Oz Bottle of Hand Sanitizer Spray - eBay But trace . 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. 75612-101-25 FDA tested product; contains acetaldehyde and acetal contaminants. 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. 71120-112-05 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. 75612-101-05 71120-611-07 FDA Recalls 149 Hand Sanitizers Due to "Toxic" Methanol - Hand McKesson Brand #53-28037-18. Company tested product; contains benzene. Suave deodorant recall 2022: Affected products. 74046-001-09 79279-420-02 Do not use these hand sanitizers according to FDA - The Washington Post Shop Target for hand sanitizer refill you will love at great low prices. 75612-101-15 74416-002-01 Best spray: Bare Hands Hand Sanitizer. 75821-002-01 Travel hand sanitizer in a convenient 8 oz. 78378-888-04 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 . 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. No water required for user's convenience. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. 74530-011-04 breathe vapors or spray mist. 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. Since the pandemic, hundreds of kinds. 74416-003-01 74458-101-09 74046-004-07 Grapefruit Extract, 74721-0010-1 70108-039-01 79279-620-02 74046-004-10, Benzalkonium Chloride Instant Hand Sanitizer, 74046-006-01 Antiseptic. 360+ Bio-Lab Advanced Hand Fragrance Free Antimicrobial Gel, 75% alcohol, 360+ Bio-Lab Advanced Hand Sanitizer Spray, 70% alcohol, ShieldOurs Hand Sanitizer Refreshing Gel, 75% alcohol, ProtectorPlus Alcohol Hand Wipes, 75% alcohol, 78378-666-01 19 Dry Shampoos Recalled Over Cancer Risk. Check If Yours Is One of 74721-0010-6 Foshan Meixin Biotechnology Co., Ltd.; formerly, Meixin Beauty & Health Care Products Co., Ltd Past product recalls have included a themed hand sanitizer from Disney. 74046-004-03 74721-0002-6 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. 79279-421-10 Ingredients. 78378-666-07 74530-012-03 78378-888-06 Call 9-1-1 if the person is unconscious or has trouble breathing. 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. This lightweight hand sanitizer spray dries quickly and leaves hands feeling fresh and clean. Our alcohol-based hand sanitizer helps eliminate over 99.9% of many common harmful germs and bacteria. 79279-610-04 In June, the FDA warned consumers against using hand sanitizer that contains the toxic ingredient methanol . This hand sanitizer formula can be used on hands when soap and water are not available to clean hands and has no added fragrance. McKesson Brand #16-1068. 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 4/05/2023. Health Canada has issued a recall for 19 hand sanitizers because they may pose health risks. PDF Material Safety Data Sheet Maridav/Shutterstock. Product Description Suave Hand Sanitizer kills 99.9 percent of germs. Product Recalls - Walmart Drug Facts Active ingredient. 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. 75339-751-03 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. 75612-101-02 74046-001-13 $2.71 reg $3.19. found to have inadequate concentrations of ethanol are NeoNatural, Medicare Alcohol Antiseptic Topical Solution, Datsen Hand Sanitizer and Alcohol. The follow products have been recalled: All-Clean Hand Sanitizer (NDC: 74589-002-01) Esk Biochem Hand Sanitizer (NDC: 74589-007-01) CleanCare NoGerm Advanced Hand Sanitizer 75% Alcohol (NDC: 74589 . The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. This will help ensure widespread access to alcohol-based hand sanitizers that are free of contamination. Credit: Amazon. . Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution, 74663-002-04 Company did not respond adequately to multiple FDA requests for records and other information related to drug manufacturing, product quality and questions regarding possibility of methanol contamination which cannot be ruled out; after FDA recall recommendation, the firm announced a voluntary recall on 10/18/2022; FDA issued a warning letter on 12/20/2022. 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. FDAs investigation of methanol in certain hand sanitizers is ongoing. 78378-888-03 First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. Do not get into eyes. Dry shampoo recall: What is benzene, the chemical of concern? | CTV News FDA tested product; contains unacceptable levels of acetaldehyde and acetal; after FDA contacted the firm, firms testing identified benzene in another product. Products that are fraudulently marketed as FDA-approved since there are no hand sanitizers approved by FDA. 75288-100-06. Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. 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. Topical Solution. 06/23/2021. 74046-001-11 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. This dry shampoo recall was at least the sixth recall this year involving benzene, according to the F.D.A.'s data. Benzene may cause certain types of cancer in humans. 0 items. Conagra Brands, Inc. 55028-007-01 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.
