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Cleaner Hand Sanitizer - recalled due to Potential Presence of Methanol (Wood Alcohol), United States

1 year ago

United States

Company name: Estado de México, México, DMM VISSION, S.A. de C.V
Brand name: Cleaner
Product recalled: Cleaner Hand Sanitizer
Reason of the recall: Potential Presence of Methanol (Wood Alcohol)
FDA Recall date: September 30, 2020
Recall details: Company Announcement Estado de México, México, DMM VISSION, S.A. de C.V. is voluntarily recalling five lots of Cleaner Hand Sanitizer, 500 mL and 1,200 mL plastic clear bottles with white tops currently in US distribution to the consumer level. This recall is being initiated out of abundance of caution due to detection of methanol (wood alcohol) in hand sanitizer sample manufactured at the same facility. 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 accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date DMM VISSION has not received reports of adverse events related to this recall. The product is used as a hand sanitizer and are packaged in 500ml and 1200ml plastic clear bottles with white tops. The lot numbers are LC2020407, LC2020408, LC2020502, LC2020504, LC2020507.  This product was first distributed nationwide to wholesale distributors on April 27, 2020 and finished on June 9th, 2020. The recalled products are as follows:
Check the full recall details on fda.gov
Source: FDA

101


Related Reports

Company name: Essaar Inc.
Brand name: Soho Fresh
Product recalled: 70% Rubbing Alcohol
Reason of the recall: Contaminated with Methanol
FDA Recall date: January 04, 2021
Recall details: Company Announcement Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol in 33.81 oz. clear... See More plastic bottles to the consumer level. FDA analysis of the product revealed it is contaminated with methanol. 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 accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, Essar Inc. has not received any reports of adverse events related to this recall. The product is used as an external purpose use rubbing alcohol and is packaged in 33.81 oz. clear plastic bottles with lot number 200528303 and UPC 7502268987367.

Soho Fresh was distributed nationwide to retail stores. Essaar Inc. is notifying its distributors and customers by email and mail and is arranging for the return of all recalled product to Essaar Inc. Consumers that have product which is being recalled should stop using and discard or return to place of purchase or to Essaar Inc. contacting via email or phone or mailing address mentioned above for arrangements of return. Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund or call Essaar Inc. at 201-647-7606 Monday to Friday 9am to 5pm, Eastern Standard Time. Essaar Inc. can also be reached via email at essaarinc@yahoo.com.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or 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 form or 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. FDA’s update  

Check the full recall details on fda.gov

Source: FDA
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103


Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 19, 2021
Recall details: Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (“Dibar”) is voluntarily recalling... See More all Dibar Labs Hand Sanitizer packaged in 8oz and 16 oz bottles, respectively, to the consumer level (see Label 1 below). Dibar is also voluntarily recalling ProtectoRx Hand Sanitizer packaged in 2oz and 16oz fluid ounce bottles, respectively, to the consumer level (see Label 2 below), as well as all Advance Hand Sanitizer packaged in 16 oz bottles, likewise, to the consumer level (see Label 3 below). These products are being recalled after testing conducted by our firm revealed the presence of 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 the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

To date, the company has not received any reports of adverse reactions related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available.

The affected bottles of hand sanitizer include a twelvedigit lot code printed on the bottle near the base. The products can be identified by the label image provided at the end of this release. Products labeled as Dibar Labs Hand Sanitizer were distributed nationwide in the USA through S.E.N.D. LLC and its customers. Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers. Products labeled as Advance Hand Sanitizer were distributed in the USA through RGV HEALTH SERVICES LLC DBA VALLEY and its customers.

Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by letter and asked that they remove the recalled products from commerce immediately if they still possess inventory.

Consumers, distributors and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this 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.

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

Check the full recall details on fda.gov

Source: FDA
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101


Company name: Prairie Wolf Spirits, Inc.
Brand name: Prairie Wolf Distillery
Product recalled: Hand sanitizer packaged in 16.9 fluid ounce and 20 fluid ounce containers that resemble water bottles
Reason of the recall: Packaged in containers resembling water bottles
FDA Recall date: June 22, 2021
Recall details:... See More Oklahoma City, Oklahoma, Prairie Wolf Spirits, Inc. is voluntarily recalling all lots of Prairie Wolf Distillery hand sanitizer packaged in 16.9 fluid ounce and 20 fluid ounce containers that resemble water bottles to the consumer level. The recall does not affect any other hand sanitizer products from Prairie Wolf Distillery. The product poses a risk of ingestion.

Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal.

Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.

To date, Prairie Wolf Spirits has received no reports of adverse reactions related to this recall. The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 16.9 ounce (UPC 6000331899) and 20 ounce plastic bottles (UPC 6000365984) that resemble water bottles. The product can be identified by the bottle’s labels pictured. The product was distributed to selected customers and consumers nationwide in the United States.

Prairie Wolf Spirits is notifying its customers by mail and is arranging for return or replacement of all recalled products. The product was sold from a temporary retail location located at 111 E. Oklahoma Avenue, Guthrie, Oklahoma 73044. Additionally, it was available on the manufacturer’s website, but there were limited sales. Prairie Wolf Spirits also donated the products from its Guthrie warehouse. Consumers that have the product which is being recalled should stop using it and return it to the Prairie Wolf Spirits distillery, 124 E. Oklahoma Avenue, Guthrie, Oklahoma, or discard it.

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

Check the full recall details on fda.gov

Source: FDA
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101


Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Hand sanitizer and hand sanitizing wipes
Reason of the recall: Microbial contamination
FDA Recall date: June 22, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan, is providing an additional 5 label illustrations and product sizes... See More for customers that might not have been able to clearly identify containers of Non-Alcohol Hand Sanitizer products that were added to the voluntary recall initiated on March 24, 2021, and expanded by the April 10 and May 14, 2021 notices. To avoid any confusion, this press release provides copies of label illustrations for the recalled products.

Durisan Non Alcohol Antimicrobial Hand Sanitizer products became contaminated with a common municipal water supply borne bacteria, Burkholderia contaminans. Use of a hand sanitizer contaminated with Burkholderia contaminans, generally considered to be of low virulence, can range from no reaction to possible infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems.

To date, no qualified reports of adverse reactions have been reported related to this recall.

The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available. The list of the lot numbers of the recalled products, which have a 24-month expiration, is included below.

Consumers and customers in possession of Durisan Non Alcohol Antimicrobial Hand Sanitizer products with these numbers in any form factor are encouraged to contact Durisan to return it.

The product is packaged in sizes ranging from 18mL credit card to 1-gallon containers. The lot number can be found in black print on the bottom of the package. Durisan Antimicrobial Solutions Hand Sanitizer Sizes With the Following Identification

- Volume mL: 18. Volume oz: 0.61. UPC: 8 52379 00614 1. NDC: 71120-112-01.
- Volume mL: 50. Volume oz: 1.69. UPC: 8 52379 00634 9. NDC: 71120-611-20.
- Volume mL: 118. Volume oz: 4. UPC: 8 52379 00612 9. NDC: 71120-112-10.
- Volume mL: 236. Volume oz: 8. UPC: 8 52379 00635 6. NDC: 71120-112-11.
- Volume mL: 250. Volume oz: 8.45. UPC: 8 52379 00611 0. NDC: 71120-611-03.
- Volume mL: 300. Volume oz: 10. UPC: 8 52379 00697 4. NDC: 71120-112-08.
- Volume mL: 550. Volume oz: 18.59. UPC: 8 52379 00620 2. NDC: 71120-112-06.
- Volume mL: 1000. Volume oz: 33.81. UPC: 8 52379 00610 3. NDC: 71120-112-05.
- Volume mL: 3785. Volume oz: 128. UPC: 8 52379 00621 9. NDC: 71120-611-05.
- Volume mL: 160 Ct Wipe. Volume oz: 5.63. UPC: 8 52379 00631 8. NDC: 71120-111-01.
- Volume mL: 80 Ct Wipe. Volume oz: 2.81. UPC: 8 52379 00632 5. NDC: 71120-111-03.
- Volume mL: 240 Ct Wipe. Volume oz: 8.44. UPC: 8 52379 00633 2. NDC: 71120-111-03.

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

Check the full recall details on fda.gov

Source: FDA
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101


artnaturals is voluntarily recalling ten manufacturing lots of artnaturals 8oz Scent Free Hand Sanitizer. FDA testing identified 8oz bottles of Scent Free Hand Sanitizer from a single manufacturing lot: G20128A, contained several impurities. Upon being contacted by the FDA, artnaturals responded immediately to proactively address the matter... See More out of an abundance of caution. After multiple communications with the FDA, the two groups have mutually agreed that artnaturals will issue a voluntary recall of 10 manufacturing lots of 8oz Scent Free Hand Sanitizer.

Exposure to the impurities found can happen naturally in our surrounding environments through inhalation, oral consumption and skin absorption. Long term exposure could result in cancers-including leukemia, cancer of the bone marrow and blood disorders.

To date, artnaturals has not received any reports of adverse events related to this voluntarily recalled product. The product is used to remove germs on hands that may cause illness when soap and water are not available and is packaged in 8 oz clear bottles.

The voluntarily recalled ten manufacturing lots of artnaturals 8oz bottles of SCENT FREE hand sanitizer are as follows:

- MFG Date: 05-05-2020. MFG LOT #: G20126E. MFG Batch #: 8737. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-06-2020. MFG LOT #: G20127D. MFG Batch #: 8730. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-06-2020. MFG LOT #: G20127A. MFG Batch #: 8730. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-06-2020. MFG LOT #: G20127A. MFG Batch #: 8737. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-06-2020. MFG LOT #: G20127E. MFG Batch #: 8733. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-07-2020. MFG LOT #: G20128D. MFG Batch #: 8735. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-07-2020. MFG LOT #: G20128F. MFG Batch #: 8739. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-07-2020. MFG LOT #: G20128A. MFG Batch #: 8733. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 5/7/2020r. MFG LOT #: G20128A. MFG Batch #: 8733. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 5/8/2020r. MFG LOT #: G20129B. MFG Batch #: 8735. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 05-08-2020. MFG LOT #: G20129C. MFG Batch #: 8739. EXPIRE DATE: 05-01-2022. UPC # 816820028205.
- MFG Date: 5/9/2020r. MFG LOT #: G20130B. MFG Batch #: 8735. EXPIRE DATE: 05-01-2022. UPC # 816820028205.

The product can be identified by the pictures below.

Product purchased from Walmart, Target, Costco, RiteAid, Publix, HEB and Amazon were not affected. artnaturals has notified the affected retailer by letter and arranged a return of all affected product. Consumers that have this recalled product should stop using and appropriately discard it.

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

Company name: artnaturals
Brand name: artnaturals
Product recalled: Scent Free Hand Sanitizer
Reason of the recall: Due to Presence of Impurities
FDA Recall date: October 27, 2021

Check the full recall details on fda.gov

Source: FDA
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102


FOR IMMEDIATE RELEASE – November 19, 2021 – American Screening LLC of Shreveport, Louisiana is voluntarily recalling 153,336 units of Hand Sanitizer, containing 70% ethyl alcohol gel to the consumer level. The hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk... See More of consumption.

Risk Statement: Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. To date, American Screening LLC has not received any reports of adverse events related to this recall.

The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in an eight ounce bottle. The affected hand sanitizer lots include the following expiration dates of 5/21/2022 and 05/24/2022 for black capped bottles and no lot numbers or expiration dates for clear capped bottles. The product can be identified by its shape (small water bottle), with a black flip top cap or clear cap with blue pouring spout with the weight of measure of eight (8) ounces/237mL, UPC 8 4005051579 2.

The Hand Sanitizer was sold to customers & distributors Nationwide via the internet at americanscreeningcorp.com and/or in-house sales.

Consumers & distributors that have this hand sanitizer which is being recalled should stop distribution/use and return to place of purchase or discard. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to ingesting the hand sanitizer packaged in the 8 oz. water bottle style.

Company name: American Screening LLC
Brand name: American Screening
Product recalled: Hand Sanitizer
Reason of the recall: Hand sanitizer is packaged in 8 oz. containers that resemble water bottles posing a risk of consumption
FDA Recall date: November 19, 2021

Check the full recall details on fda.gov

Source: FDA
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Village of Niobrara still under a Boil Water Advisory.

Source: twitter.com
Source publication date: 2021 11 27 See Less


Due to the strong winds of Santa Ana and the extremely dry conditions, San Diego Gas & Electric cut off power to thousands of customers (mostly East County and backcountry areas) on Thanksgiving and Friday. As of 2:15 pm on Friday Reported utility 1,142 customers in the... See More community, including Alpine, Jamal and Boulevard, turned off their wires as Santa Ana winds blew through San Diego County for two consecutive days.

Source: californianewstimes.com
Source publication date: 2021 11 27
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East Richland Water System is issuing a boil advisory until further notice.

Source: twitter.com
Source publication date: 2021 11 27 See Less


Boil water notice issued for 293 homes in Black Hammock Service Area

Source: twitter.com
Source publication date: 2021 11 27 See Less