Open Book Extracts Issues Voluntary Nationwide Recall of All Lots of Always Be Clean Hand Sanitizer and Just Hand Sanitizer that are Labeled to Contain Methanol - 9/2/20

Summary

Company Announcement Date:

August 29, 2020

FDA Publish Date:

August 31, 2020

Product Type:

Drugs

Reason for Announcement:

Products labeled to contain methanol

Company Name:

Open Book Extracts

Brand Name:

Always Be Clean, Just

Product Description:

Hand Sanitizer

Company Announcement

Open Book Extracts (OBX) is voluntarily recalling to the consumer level all lots of Always Be Clean Hand Sanitizer and Just Hand Sanitizer that are labeled to contain methanol.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

OBX sources hand sanitizer from a leading global chemical and ingredient distributor, and has verified through a third-party lab that the hand sanitizer does not contain reportable levels of methanol. The supplier updated the Safety Data Sheet (SDS) to remove methanol since it is below the reportable level, and we updated the labels accordingly.

These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available.

The mislabeled hand sanitizer was packaged in single-use packets and multi-count boxes using the following NDC and Lot codes:

Name of Product NDC Size UPC Lot
Always Be Clean hand sanitizer 75091-2020-1
75091-2020-2
75091-2020-3
Single snaps
100 Count
25 Count
375091202016
375091202023
375091202030
ES8-200514
Just Hand Sanitizer 78065-2020-1
78065-2020-2
Single Snaps
100 Count
703123998659
703123998598
ES9-200610

The mislabeled hand sanitizer was packaged from May 14, 2020 through June 1, 2020 and sold from May 15, 2020 through July 16, 2020 Nationwide in the USA to businesses for internal use.

OBX has notified all distributors via phone and email and is replacing all of the mislabeled product. While OBX believes that all mislabeled units have been recovered or, in the case of Just Hand Sanitizer, were relabeled prior to sale, anyone with questions regarding this recall or are in possession of Just Hand Sanitizer or Always Be Clean Hand Sanitizer from the above-listed lots that list methanol as an inactive ingredient may contact Open Book Extracts at handsanitizer@openbookextracts.com or 917-536-1194 (9 a.m.- 5 p.m. ET) to replace the hand sanitizer free of charge.

Distributors or businesses that have product labeled to contain methanol should stop distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

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.

Link to FDA Update

Company Contact Information

Consumers:

917-536-1194

 handsanitizer@openbookextracts.com

Media:

440-413-0371

 media@openbookextracts.com

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/open-book-extracts-issues-voluntary-nationwide-recall-all-lots-always-be-clean-hand-sanitizer-and?utm_campaign=Open%20Book%20Extracts%20Issues%20Voluntary%20Nationwide%20Recall%20of%20All%20Lots%20of%20Always%20Be%20Clean%20Hand%20Sanitizer&utm_medium=email&utm_source=Eloqua

 

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* 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.
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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 http://www.fda.gov/opacom/7alerts.html, and the United States Department of Agriculture (USDA) at http://www.fsis.usda.gov/Fsis_Recalls/index.asp. Additionally, members can often receive information on national, state, and local recalls by contacting their local health departments.

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