Albek de Mexico S.A. de C.V. Issues Voluntary Nationwide Recall of All Hand Sanitizers Due to Potential Presence of Undeclared Methanol - 8/20/20


Company Announcement Date:

July 31, 2020

FDA Publish Date:

August 18, 2020

Product Type:


Reason for Announcement:

Undeclared Methanol

Company Name:

ALBEK de Mexico S.A. de C.V.

Brand Name:

Nuuxsan, Modesa, more

Product Description:

Hand Sanitizer

Company Announcement

SAN JUAN del RIO QUERETARO, Mexico — ALBEK de Mexico S.A. de C.V. is voluntarily recalling all lots and all brands of hand sanitizer currently in US distribution to the consumer level. The products were manufactured between November 7, 2019 and June 28, 2020.

This recall is being initiated out of an abundance of caution due to detection of methanol in hand sanitizer samples manufactured by Albek when product was presented for import into the United States.

Risk Statement: Substantial methanol exposure could result in serious health effects (including nausea, diarrhea, vomiting, severe abdominal pain, headache, blurred vision, permanent blindness, seizures, coma, nervous system damage) or death. Persons using methanol-based products on their hands may be at risk. Young children who accidently ingest them and adolescents and adults who drink such products are most at risk for methanol poisoning. To date, there have been no reports of serious adverse events related to the products in the scope of this recall.

Recalled Products: The products are labeled for use as a hand sanitizer (or “antiseptic”) and are packaged for several nationwide distributors in a variety of formats as indicated in the table as follows:

BRANDS: Nuuxsan Modesa Assured Assured Next
Product Name Nuuxsan Instant Hand Sanitizer Modesa Hand Sanitizer with Moisturizers and Aloe Vera Assured Hand Sanitizer Vitamin E and Aloe Assured Hand Sanitizer Aloe Vera Next Hand Sanitizer
NDC 72758-005-02, 72758-001-08 72758-011-23 72758-010-23 72758-009-23 50066-605-08
Sizes 8 fl oz 8 fl oz 8 fl oz 8 fl oz 8 fl oz
UPC 713620000175 32251380426 639277928597 639277928610 650240053573
Affected Lots All Lot #s 1931104AL 1931101AL 1931102AL The affected lots end in:
1001, 1002, 1003, 1004, 1005

These products were distributed nationwide in the United States beginning on November, 15 2019.

Albek is partnering with its distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled products. Consumers, distributors, and retailers that have product which is being recalled should stop use or distribution and return to place of purchase.

Consumers with questions regarding this recall can contact Albek de Mexico S.A. de C.V. during the business hours business hours: 9:00am – 5:00pm (CT)


Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using these products.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

  • Complete and submit the report Online
  • Regular Mail or Fax: Download formor call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.


Company Contact Information


Albek de Mexico S.A. de C.V.



Manuel Beltrán M.

52 1 427 101 8200 ext. 102



* We believe that none of the product being recalled were processed or offered through the national office
* We strongly encourage you to notify your agencies within one business day from receipt of this notice.
* ALL cased and uncased inventories, both at the member level and agency level, need to be checked. This product may have entered member and agency warehouses through salvage, local donations, TEFAP, local purchases, retail pickups, food drives, or other avenues.
* For additional local details, please contact the Health Department(s) for the area(s) your food bank serves.
About Feeding America Recall Notices

The Feeding America national office issues notifications of all national Class I and II recalls–those involving a health hazard situation in which there is reasonable probability that eating the food will cause health problems or death–and other recalls that may affect the safety of food supplied to network members.

The national office strongly encourages all member product solicitors, operations managers, and others involved in food and grocery distribution to regularly consult resources provided by the United States Food and Drug Administration (FDA) at, and the United States Department of Agriculture (USDA) at Additionally, members can often receive information on national, state, and local recalls by contacting their local health departments.