If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. 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. Drug Safety and Availability, Recalls, Market Withdrawals and Safety Alerts, Information about Nitrosamine Impurities in Medications, 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, 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, local waste management and recycling center, Centers for Disease Control and Prevention, 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.

And one of those hand sanitizers was sold throughout the Kroger superchain, comprised of Kroger and 14 other chains. The Food and Drug Administration has updated its recall list to include 149 different hand sanitizers due to failing standards on randomized tests.

Retailers should contact the distributor or manufacturer for specifics on receiving a credit/refund for the returned product, DLCA said. Additionally, FDA reminds consumers that no drugs, including hand sanitizers, are approved to prevent the spread of COVID-19. ▪ Albek de Mexico recalled Next Hand Sanitizer, lot numbers that ended in 1001, 1002, 1003, 1004 or 1005; NuuxSan Instant Antibacterial Hand Sanitizer, all lots; Assured Hand Sanitizer with Vitamin E and Aloe, lot No. WICO Gearing Up to Reopen Port to Cruise Ships as Early as January, BREAKING NEWS : Has been tested and is found to have microbial contamination. FDA encourages health care professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDA’s 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 products that are labeled to contain ethanol (also known as ethyl alcohol) but that have tested positive for methanol contamination. This testing method can be used to help assure hand sanitizers contain the correct ingredients and do not contain harmful levels of impurities. The agency will provide additional information as it becomes available. Is Your Hand Sanitizer on FDA’s List of Products You Should Not Use? Genomma Lab USA Expands Recall of NEXT Hand Sanitizer Product may contain unsafe levels of methanol.

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