is gsd hand sanitizer recalled

Posted: Jul 13, 2020 / 07:57 AM PDT. Safety officials at the Food and Drug Administration are warning Americans that not all hand sanitizers are made equal,. EO Hand Sanitizer Gel. 80969-007-01 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. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. Harmonic Nature S de RL de MI (Mexico) FDA tested product; contains 1-propanol; FDA recommended the company recall on 8/12/2020; added to import alert to stop products from entering the U.S. on 8/20/2020; product voluntarily recalled on 8/14/2020. GSD Liquid Hand Sanitizer Item: #2353632 4.2 (14) $1.97 Save 15% with MILITARY STAR Plans Size: 33.8 oz. 75821-002-01 Updated: Jul 13, 2020 / 11:49 AM PDT. 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). Medically Minded Hand Sanitizer Gel V-KLEAN DermX70 Hand Sanitizer (only includes 250mL, 500mL and 1000mL sized packages) V-KLEAN Hand Sanitizer Gel V-KLEAN Hand Sanitizer Gel. Hand sanitizer recalled due to undeclared methanol Product Number: 849AB/BA Product Name: Moisturizing Hand Sanitizer Issuing Date: April 22, 2020 Revision Date: None Revision Number: 0 Safety Data Sheet The supplier identified below generated this SDS using the UL SDS template. Distributors often do not identify the manufacturer on the product label and are not required to do so under federal law. GSD All Purpose Liquid Sanitizer & Disinfectant MEGA REFILL SIZE 1.75L (59.2 OZ) 80% ALCOHOL GSD All Purpose Liquid Sanitizer & Disinfectant FAMILY SIZE 1L (33.2 OZ) 80% ALCOHOL GSD All Purpose Liquid Sanitizer & Disinfectant POCKET SIZE 375mL (12.6 OZ) 73% Alcohol - Gel Sanitizer & Disinfectant With Essential Oils 73% ALCOHOL One product is also improperly labelled. $8.19. Contact your local waste management and recycling center for more information on hazardous waste disposal. 74046-006-04 A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. Company tested product; Product labeled as containing Isopropyl Alcohol determined to contain undeclared ethyl alcohol at sub-potent concentrations; FDA recommended the company recall on 2/16/2022 Associated lot numbers: Company tested product lot 200423322; Product labeled as containing Isopropyl Alcohol determined to contain undeclared ethyl alcohol at sub-potent concentrations; FDA recommended the company recall on 2/16/2022. Health Canada recalls 9 more hand sanitizers over safety risks In the letter, company asked the FDA to recall the contaminated batches of hand sanitizer, conduct an investigation of the products, and provide information to the public, among other things. 74046-006-10. Individual Warp Wipes can use anywhere you need to clean hands or there's no water available. Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. Report any health product adverse events or complaints to Health Canada. 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. 74530-011-08, 74530-013-01 75821-001-02 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. GSD Advanced Hand Sanitizer Drug Facts Active ingredients Ethyl alcohol 70% v/v Purpose Antimicrobial Use It was only four months ago that hand sanitizers became one of the hottest products to fly off the shelves around the world to help stave off the coronavirus. We will ensure that your family stays protected from dust. Scentsational Soaps & Candles, Inc. issued a voluntary recall on the spray . 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. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. 74721-0002-7 74530-015-04 74530-012-03 Durisan voluntarily recalled its hand sanitizer product on March 24, 2021 and expanded their recall on April 16, 2021. The affected products are packaged in 4-ounce, 8-ounce, 16-ounce, and one-gallon bottles and were sold through online sales and retail . Is packaged in a container that resembles a food/beverage container that presents increased risk of accidental ingestion. 08/11/2020. 79279-420-04 Hand sanitizer recall: FDA says Medically Minded brand found to contain Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. Anti-Bac Hand Sanitizer 70% alcohol, Born Basic. 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. That chemical, according to the recall posted on the U.S. Food and Drug Administration's website, is . The company announced the recall on Mar. FDA hand sanitizer recall widens to over 100 products Consumers who have products on this list of hand sanitizers should immediately stop using the product and dispose of it, ideally in a hazardous waste container. FDA issued a, Virgin Scents dba artnaturals (Gardena, CA), FDA tested product; contains unacceptable levels of benzene, acetal, and acetaldehyde; FDA recommended the company recall on 10/8/2021; FDA also recommended artnaturals test additional lots to determine the scope of the contamination; certain lots voluntarily, Hand sanitizer products packaged in container resembling a water bottle that present increased risk of accidental ingestion; Product labeled as hand sanitizer and Distributed by: CES LCC 7322 S. Rainbow Blvd. 74721-0002-6 74046-001-03 79279-421-09 First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. FDA remains vigilant and will continue to take action when quality issues arise with hand sanitizers. 71120-612-07 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. Methanol is not an acceptable ingredient for any drug and should not be used due to its toxic effects. 74046-001-11 74046-001-07 Lukas Flippo, Photo Editor. UL did not test, certify, or approve the substance described in this SDS, and 74530-012-07 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. An independent pharmacy and lab conducted a study of hand sanitizers sold during the pandemic and found that samples from 44 of them contained benzene, a chemical known to cause leukemia. GSD All-Purpose Anti-Bacterial Wipes | 80 Wipes per Packet 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. Before sharing sensitive information, make sure you're on a federal government site. 74721-0010-8 Health Canada has issued a recall for 19 hand sanitizers because they may pose health risks. 74721-0001-7 The agency urges consumers not to use these subpotent products and has expanded its list to include subpotent hand sanitizers, in addition to hand sanitizers that are or may be contaminated with methanol. CLARKSBURG, W.Va. (WBOY) A hand sanitizer that was sold over the internet nationwide is being recalled because the company that manufactured it says it may have been contaminated with a toxic chemical. 71120-612-06 GSD Hand Sanitizer, Hand Sanitizer, 33.8 Ounce Brand: GSD Hand Sanitizer 3 ratings Currently unavailable. Add to Cart Overview GSD Liquid Hand Sanitizer kills more than 99.99% of the most common germs. 74046-001-04 74721-0001-5 Mint Oil 74721-0010-5 GSD Advanced Hand Sanitizer - 80% Alcohol Based - ( 1 Liter) $15.50 + $11.63 shipping. FDAs investigation of methanol in certain hand sanitizers is ongoing. Do not use these hand sanitizers according to FDA - Washington Post The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. Acetal can irritate the upper respiratory tract, eyes, and skin. 74721-0010-6 The temporary guidances have also been updated to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities. Ultra Defense Sani + Smart Team Reaches out to White House Aloe Vera Based Hand And Skin Purifying Gel. In most . Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? List of antiseptic or antibacterial skin cleansers or hand sanitizers meeting Health Canada's requirements for safety, effectiveness and quality, for use against coronavirus (COVID-19). COVID-19: List of hand sanitizers authorized by Health Canada - Canada.ca Call 9-1-1 if the person is unconscious or has trouble breathing. 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. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. Germ-X Gel Hand Sanitizer, Bottle of Gel Hand Sanitizer with Cap, Original Scen. [10/4/2021]FDA has tested certain artnaturals scent free hand sanitizer labeled with DIST. 74046-001-13 74721-0001-2 Stay clean and germ free. World Health Organization formula. 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. 80969-040-04, PFA Stronghold Hand Sanitizer 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. 79279-620-01 by artnaturals Gardena, CA 90248 and found unacceptable levels of benzene, acetaldehyde, and acetal contaminants. Hand sanitizer recalled over potential methanol contamination Specifications Value of Product Features Most Helpful Favorable Review Good stuff ! The new additions cont Alcohol Free Disinfectant, Safe Cleaner Plus 74721-0002-3 74046-006-02 GSD Advanced Hand Sanitizer. 74530-015-02 74046-006-06 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. Do not pour these products down the drain or flush them. 74721-0001-9 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. If You're Using This Hand Sanitizer, Stop Immediately - Best Life Cultivation Republic (Clearwater, Florida). The FDA has published a long list of hand sanitizers that they do not recommend for use. Animal studies indicate that the central nervous system depressant effects of 1-propanol are 2 to 4 times as potent as alcohol (ethanol). Consult your health care professional if you have used any of these products and have health concerns. Artnaturals has been added to the list. 71120-611-08 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. Some Hand Sanitizers Made During the Pandemic Have - Insider 75339-751-05 74046-001-14 Product purported to be made at the same facility that produced an acetaldehyde and acetal contaminated product. 74721-0001-0 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. 74721-0020-9, 71120-112-01 Drivergent Hand Sanitizer, Alcohol Antiseptic 80% Topical Solution, Antiseptic Hand Rub, Non-Sterile Solution. 74046-001-16 Hand sanitizer recall: FDA list of 'do not use' products - New York Post There's a nationwide spray hand sanitizer recall on 11 products that were sold at Ulta, TJ Maxx, and Marshalls stores. 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). Canada's health agency has added three more hand sanitizer products to its growing list of 48 recalled items which began in the spring of 2021. 79279-620-03 04:20. 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. Alcohol-based hand sanitizers that are contaminated with methanol are subject to adulteration charges under the FD&C Act. Health Canada warns about certain hand sanitizers that may pose health 74046-001-09 Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. Disney-branded hand sanitizers recalled due to carcinogen | CNN Do not pour these products down the drain or flush them. 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. 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 08/16/2022. 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. According to the FDA, you should use an alcohol-based hand. Innovaciones Tecnologicas Concar, SA de CV 75821-001-04 FDA tested product; contains methanol; product voluntarily recalled on 11/5/2022. Sun Wave Antiseptic Hand Sanitizer Alcohol Antiseptic 70% Enriched with Aloe Clean Scent. 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 This comes after a series of recalls related to. Category: Hand Sanitizer. Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 74721-0001-4 79279-521-03 FDA Adds 4 Brands Of Hand Sanitizer To Growing Recall List (NEXSTAR) American Screening LLC is voluntarily recalling 153,336 units of hand sanitizer that are packaged in containers that look like water bottles and pose a risk of consumption. CNN Two lots of Disney-branded hand sanitizer featuring Mickey Mouse and baby Yoda from The Mandalorian have been voluntarily recalled by Best Brands Consumer Products, according to a. 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. 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. 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 . 79279-420-02 FDA is not aware of any adverse events related to Durisans hand sanitizer products. 74046-006-09 79279-520-08 Topical Solution. Hand sanitizer is a great way to keep your hands clean while in public. The ITECH 361 recall is for 18,940 bottles of All Clean hand sanitizer sold in one-liter bottles with UPC Code 628055370130. FDA updates on hand sanitizers consumers should not use | FDA The dangers of drinking any hand sanitizer under any conditions. 80969-020-03 Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. 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. 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). Hand Sanitizer Topical Solution, Alcohol Antiseptic 80%, 75293-001-02 74721-0001-6 Some of the products have already been recalled. 74721-0010-7 FDA tested product; contains unacceptable levels of acetaldehyde and acetal; FDA recommended the company recall on 10/18/2022; Company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality and scope of the contamination. 9 best hand sanitizers meeting CDC guidance - NBC News The newest recalled hand sanitizers are: 74530-011-02 Free shipping. Skin or eye exposure to 1-propanol can result in irritation, and rare cases of allergic skin reactions have been reported. This recall is being conducted with the knowledge of the FDA. Product contains methanol based on information provided by the manufacturer. The agency tweeted on Monday about the two latest recalls. 74530-011-04 [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. GSD Disinfecting Sanitizing Wipes can be used for everyone. Never eat or drink hand sanitizers, as swallowing even small amounts can be dangerous or fatal. A hand sanitizer made by nanoMaterials Discovery Corp. has been recalled because the U.S. Food and Drug Administration said it "may exceed FDA limits for methanol." Snowy Range Blue alcohol . 79279-421-07 74046-001-02 You should look for lot number 1166A and expiration date 6/18/2023 on the container. If You're Using This Hand Sanitizer, Stop Immediately, FDA Warns - Yahoo! 74721-0010-9 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. The agency urges consumers not to use this contaminated product and has added artnaturals hand sanitizer products to thelistof hand sanitizers consumers should not use. 7 and the U.S. Food & Drug Administration (FDA) posted the recall notice on the same date.