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. The pouch is resealable to ensure your wipes are always fresh. Pleasant scent and safe for sensitive 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 09/27/2022; product voluntarily recalled on 9/27/2022. Free shipping. 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. 74530-011-05 74530-011-02 74046-001-12 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. GSD Advanced Hand Sanitizer Drug Facts Active ingredients Ethyl alcohol 70% v/v Purpose Antimicrobial Use The four products added to the recall list. An official website of the United States government, : 33.8 oz. Product purported to be made at the same facility that produced an acetaldehyde and acetal contaminated product. 79279-620-04 GSD Disinfecting Sanitizing Wipes can be used for everyone. GSD Advanced Hand Sanitizer - 80% Alcohol Based - ( 1 Liter) $15.50 + $11.63 shipping. 74530-015-04 74721-0020-8 The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. A hand sanitizer that was sold over the internet nationwide is being recalled because it may have been contaminated with toxic methanol. The affected products are packaged in 4-ounce, 8-ounce, 16-ounce, and one-gallon bottles and were sold through online sales and retail . 75339-751-03 If soap and water are not readily available, the Centers 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). To help limit the spread of COVID-19, wash your hands often with soap and water for at least 20 seconds. 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. Updated: Jul 13, 2020 / 11:49 AM PDT. MIAMI (CBSMiami) - The Food and Drug Administration has added four brands of hand sanitizer to a list of more than 75 that have been recalled. 79279-521-04 The test method for methanol described in the USP Alcohol Monograph can also be used to test for methanol contamination in isopropyl alcohol. Hand sanitizer products packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 09/08/2021. Flavor Vapors, LLC, dba: Mob Liquid Labs Transliquid. For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. 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. 74530-013-05 FDA will consider revising the list as appropriate. 04:20. Real Clean Distribuciones has recalled its Scent Theory Keep Clean and Keep It Clean, Born Basic, and Lux Eoi hand sanitizers, The Miami Herald found. 74721-0010-7 79279-520-06 We don't know when or if this item will be back in stock. Hand Sanitizer Topical Solution, Alcohol Antiseptic 80%, 75293-001-02 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. FDA recommended the company recall all drug products on 12/12/2022. 79279-520-08 74046-001-18 Kleanz Antibacterial Hand Sanitizer Advanced, Be Safe Hand Sanitizer (labeled with Model: BF-HGXXXX-09 where XXXX changes based on packaging size), Product manufactured at a facility that did not respond to multiple FDA requests for recordsrelated to drug manufacturing and product qualityeven afterreceiving a warning letter. 74721-0010-9 71120-117-02, 75821-001-01 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. Germ-X Gel Hand Sanitizer, Bottle of Gel Hand Sanitizer with Cap, Original Scen. The FDA listed the following products in its warning: All-Clean Hand Sanitizer (NDC: 74589-002-01) Esk Biochem Hand Sanitizer (NDC: 74589-007-01) CleanCare NoGerm Advanced Hand Sanitizer 75% . 74046-001-11 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. About this item No animal testing for beauty products 3rd-party certification required for organic claims on body care products Product Description Body Care Product details Additionally, FDA reminds consumers that no drugs, including hand sanitizers, are approved to prevent the spread of COVID-19. 74721-0020-5 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. 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). Safety officials at the Food and Drug Administration are warning Americans that not all hand sanitizers are made equal,. 74721-0002-2 Hideout Hand Sanitizer non-sterile solution Alcohol Antiseptic 80% Topical Solution. Grapefruit Extract, 74721-0001-1 Free shipping. Hand sanitizer recall: FDA expands list of 'toxic' sanitizers to avoid over methanol risk by: Alexa Mae Asperin. The .gov means its official.Federal government websites often end in .gov or .mil. Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 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. Suite #166 Las Vegas, NV 89139" FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product, Hand sanitizer products packaged in container resembling a water bottle that present increased risk of accidental ingestion;Product labeled as handsanitizer and Distributed by: CES LCC 7322 S. Rainbow Blvd. The site is secure. 74046-004-08 Health Canada has suspended the product licence for two of . It also reported that Target sold Born Basic Anti-Bac Hand Sanitizer, while Walmart sold Scent Theory at stores in 17 states. 74721-0020-7 80969-020-03 70% Alcohol Cleansing Gel Say Goodbye to Germs. 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. The FDA included several types of. 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; added manufacturer to, 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. Consult your health care professional if you have used any of these products and have health concerns. Add to cart. 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. 74046-006-08 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. Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. Instant action with safe ingredients - no Triclosan, Sulfates, Parabens or Synthetics. Mint Oil First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. 79279-421-08 In most . If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. Cultivation Republic (Clearwater, Florida). Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. Alcohol antiseptic 80% topical solution. 74046-001-20. 71120-611-08 Maridav/Shutterstock. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. Add to Cart Overview GSD Liquid Hand Sanitizer kills more than 99.99% of the most common germs. The company, Spartan Chemical, issued a recall for its "Lite 'n Foamy Lemon Blossom Hand Sanitizer" and "foamyiQ Lemon Blossom Hand Sanitizer" on July 1. 74046-001-08 $19.95. 74046-001-10 The agency also included an additional denaturant formula in the temporary guidances. Consumers who have been exposed to hand sanitizer containing methanol and are experiencing symptoms should seek immediate treatment for potential reversal of toxic effects of methanol poisoning. FDA tested product; contains 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): [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. Skin or eye exposure to 1-propanol can result in irritation, and rare cases of allergic skin reactions have been reported. 74530-013-06 The ITECH 361 recall is for 18,940 bottles of All Clean hand sanitizer sold in one-liter bottles with UPC Code 628055370130. On March 26, students, faculty and staff were notified in an email from Yale's Environmental Health & Safety Department, or EHS, that benzene, a substance that can cause cancer, was detected in two hand sanitizer brands distributed by Yale, CleanHands and ArtNaturals, and were asked to dispose of the hand . 75293-001-01, Coppercraft Distillery, LLC 74530-013-03 79279-610-03 FDA recommended the company recall on 06/01/2022. The agencys investigation of contaminated hand sanitizers is ongoing. While USP has not yet updated the Isopropyl Alcohol Monograph to include a specific methanol limit, FDA may consider the 200 ppm methanol limit for ethanol to also be suitable for isopropyl alcohol. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. 74046-001-06 (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 Is being recalled by the manufacturer or distributor. Recalled hand sanitizers The following products have been recalled as of July 18: ITECH 361's All Clean Hand Sanitizer, Moisturizer and Disinfectant : UPC code 628055370130. 74046-006-10. The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. Dongguan Mingyi Medical Products, Co., Ltd. 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. 79279-620-01 79279-421-07 74721-0001-3 That chemical, according to the recall posted on the U.S. Food and Drug Administration's website, is . Scentsational Soaps & Candles, Inc. issued a voluntary recall on the spray . 74721-0001-4 The agency has recalled hand sanitizers from the companies All-Clean, Eskbiochem, CleanCare, Saniderm, Lavar 70 and Good Gel, which were all manufactured by Mexico-based Eskbiochem SA de CV..
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