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Hand Sanitizer

Updated: September 5, 2020 12:01 PM
Company name: CorgioMed LLC
Brand name: Leafree
Product recalled: Hand sanitizer
Reason of the recall: Product is labeled as edible alcohol.
FDA Recall date: September 03, 2020
Recall details: CorgioMed, LLC is voluntarily recalling all lots of Leafree Instant Hand Sanitizer-Aloe Vera, within expiry to the consumer... See More level.  The products are being recalled because they are labeled as “EDIBLE ALCOHOL”. Leafree Hand Sanitizer is an alcohol-based hand rub to be applied externally to reduce bacteria on the skin when soap and water are not available.

Risk Statement: Ingesting hand sanitizer, which is intended for topical use, may 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. Young children may experience a sharp decrease in blood sugar which may result in death. Pregnant women who ingest alcohol have experienced birth defects and developmental disabilities. Nursing mothers who ingest alcohol in above moderate levels may see developmental, growth and sleep pattern damages in their babies and may experience impaired judgement and ability to safely care for their child.

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.  The labeling of this product as ‘edible alcohol’ may promote this behavior. The product is used as a hand sanitizer and is packaged in 100 ml (UPC #6970495860325), 300 ml (UPC #69705860318) and 500 ml (UPC #6970495860301) bottles. 

Product was distributed Nationwide via CorgioMed website. CorgioMed LLC is notifying its distributors and customers by email and is arranging for return or disposal of all recalled products. Distributors and Consumers with questions regarding this recall can contact CorgioMed LLC by emailing to: contact@corgiomed.comor phone: 301-978-3898 from September 1st to September 30th, 2020. 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.
Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/corgiomed-llc-issues-voluntary-nationwide-recall-all-lots-leafree-instant-hand-sanitizer-aloe-vera

Source: FDA
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Company name: AJR Trading LLC
Brand name: bio aaa
Product recalled: Hand Sanitizer
Reason of the recall: Possible presence of methanol
FDA Recall date: September 03, 2020
Recall details: AJR Trading is voluntarily recalling 2,004 units of lot 20DF8307 of bio aaa Advance Hand Sanitizer currently in... See More US distribution, packaged in 480 mL bottles, to the consumer level. This lot of bio aaa Advance Hand Sanitizer has been tested and meets all appropriate specifications and tests. However, in an abundance of caution, these units are being recalled because of possible presence of methanol in other lots of bio aaa Advance Hand Sanitizer.

Risk Statement: Substantial methanol exposure could 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 may be at risk; young children who accidently ingest them and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, AJR Trading has not received reports of adverse events related to this recall.

The product is used as a hand sanitizer to reduce bacteria when soap and water is not available and is packaged in 480 mL plastic bottles UPC 7502272121085.  AJR Trading is recalling lot 20DF8307, expiration date April 2022. The product can be identified by the images below. Product was distributed in Miami beginning in April 2020. AJR Trading is notifying its customers by phone calls, e-mails, and letters.  AJR Trading is arranging for refund and destruction of recalled products.

Consumers/distributors/retailers that have the above listed lots of bio aaa Hand Sanitizer, which is being recalled, should stop using or distributing the products immediately and mail the products to AJR Trading at the following address for refund: 814 Ponce de Leon Blvd, suite 218. Coral Gables, FL. 33134. Consumers with questions regarding this recall can contact AJR Trading by phone insert 305-302-8416 or e-mail to ajrtrading15@gmaill.com Monday to Friday from 10:00 am to 5:00 pm Central Time.

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

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

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ajr-trading-llc-issues-voluntary-nationwide-recall-bio-aaa-advance-hand-sanitizer-480-ml-bottles-lot

Source: FDA
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Company name: HARMONIC NATURE S. DE R.L. Mi
Brand name: Harmonic Nature
Product recalled: Hand sanitizer
Reason of the recall: Product contains 1 propanol
FDA Recall date: August 28, 2020
Recall details: Guadalupe, Nuevo Leon, Harmonic Nature is voluntarily recalling all 800 bottles Hand Sanitizer, 250mL, product... See More due to the potential presence of 1-propanol. The products have been tested and found to contain 1 propanol.

Risk Statement: Any amount of 1-propanol with a concentration greater than or equal to 1% by volume that is unlisted in a product labeled as an ethanol-based hand sanitizer has a reasonable probability of acute toxicity from ingestion which can cause central nervous system depression, which could result in death, permanent impairment, or necessitate medical or surgical intervention. Populations most at risk include individual with alcohol addiction and adolescents, who have been known to ingest ethanol-based antiseptic rubs intentionally to become intoxicated, as well as infants and children who may unintentionally ingest the defective product.

Harmonic Nature has not received any reports of adverse events related to this recall. The product is used as a hand sanitizer and is packaged in 250 mL plastic bottles , with UPC Code 7500462892210. The product can be identified by Harmonic Nature as a hand sanitizer Topical Solution distributed only to and currently on hold at the US custom bróker, Aquiles INC. Harmonic Nature is notifying Aquiles INC. and is arranging for return of all recalled product. Consumers with questions regarding this recall can contact Harmonic Nature by +(52) 8120 2967 03 or miguel_martinez2000@yahoo.com Monday to Friday from 8:00 am to 6:00pm central time. 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.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. CDER’s press statement

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/harmonic-nature-issues-voluntary-nationwide-recall-hand-sanitizer-due-presence-1-propanol

Source: FDA
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Company name: Nanomateriales, SA de CV
Brand name: Zanilast+
Product recalled: Hand sanitizer
Reason of the recall: Product contains 1-propanol.
FDA Recall date: August 26, 2020
Recall details: Apodaca, Nuevo Leon, Nanomateriales is voluntarily recalling all lots of ZANILAST+ GEL, Sanitizer gel, to the consumer level. FDA... See More laboratory analysis found ZANILAST+ GEL to contain 1-propanol.

Risk Statement: There is a reasonable probability of acute toxicity from ingestion which can cause central nervous system depression, which could result in death, permanent impairment, or necessitate medical or surgical intervention. Populations most at risk include individual with alcohol addiction and adolescents, who have been known to ingest ethanol-based antiseptic rubs intentionally to become intoxicated, as well as infants and children who may unintentionally ingest the defective product.

Nanomateriales, SA de CV has not received any reports of adverse events related to this recall. The product is used as a sanitizer gel, for hand washing to decrease bacteria on the skin and is packaged in 1 liter, 25 liters, and 1 gallon plastic bottles distributed from 05/29/2020 to 06/17/2020 in the States of California, New York and New Jersey.

Presentatio UPC NDC Lable
1 Liter 2 000000 531151 69912-008-01 See below
25 Liter 2 000000 531151 69912-006-01 See below
1 galon 2 000000 531144 69912-008-02 See below

Nanomateriales, SA de CV is notifying its distributors and customers by e-mail and phone and is arranging for return of all recalled products. Consumers and distributors that have ZANILAST+ GEL which is being recalled should return to place of purchase.

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nanomateriales-sa-de-cv-issues-voluntary-nationwide-recall-all-lots-zanilastgel-due-presence-1

Source: FDA
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Company name: Asiaticon SA de CV
Brand name: V-Klean, Medical Minded, Protz
Product recalled: Hand Sanitizer
Reason of the recall: Potential presence of methanol (wood alcohol) and subpotent ethanol levels
FDA Recall date: August 25, 2020
Recall details: Mexico City, Mexico, Asiaticon SA de CV (Mexico) is... See More voluntarily recalling all lots of V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel and Protz Real Protection Antibacterial Hand Sanitizer sold in 13.5, 16.9 and 33.8 ounce bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol) and subpotent ethanol levels.

Risk Statement:  Methanol has inferior antiseptic properties compared to ethanol.  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 person 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 Asiaticon SA de CV has not received reports of adverse events related to this recall. The product is used as a hand sanitizer and is packaged in plastic clear bottles with clear tops with UPC Code:

- V-Klean in 8.5 fl. oz. (250 ml) bottles: 716053704993
- V-Klean in 16.9 fl. oz. (500 ml) bottles: 716053704993
- V-Klean in 33.8 fl. oz. (1000 ml) bottles: 716053704993
- Medically Minded in 16.9 fl. oz. (500 ml) bottles: 676753003782
- Protz in 13.5 fl. oz. (400 ml) bottles: 7503019005002

The recall includes all lots.  This product was exported to different distributors nationwide. Asiaticon SA de CV is notifying its distributors by voluntary recall letter and consumers via this press release. Consumers that have the product subject to this recall should stop using and either contact Asiaticon SA de CV per the below for disposal instructions or return it to the place of purchase. Consumers with questions regarding this recall can contact Asiaticon SA de CV at direccion@asiatic-connection.com (0052 1 55 21553488). 

In the US: at 929 394 3020 (available Monday to Friday 9.30 am  6 pm eastern time) Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to 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 www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/asiaticon-sa-de-cv-issues-voluntary-nationwide-recall-v-klean-hand-sanitizer-gel-medically-minded

Source: FDA
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Company name: Grupo Asimex de Mexico SA de CV
Brand name: FLORANCE MORRIS
Product recalled: Antiseptic Hand Sanitizer, 70% Alcohol
Reason of the recall: Potential Methanol Contamination
FDA Recall date: August 20, 2020
Recall details: Company Announcement Grupo Asimex de Mexico SA de CV is voluntarily recalling... See More all lots of FLORANCE MORRIS Antiseptic Hand Sanitizer, 70% Alcohol, packaged in 8 fl oz bottles and 1L bottles to the consumer level. The products have the potential to contain methanol (wood alcohol) and be sub-potent for the ethanol content. Risk Statement: The use of sub-potent hand sanitizer products can have adverse health consequences related to infections. Ethanol levels below the label claim can result in a lack of efficacy. In addition, methanol has inferior antiseptic properties compared to ethanol. 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 person 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, Grupo Asimex de Mexico SA de CV has not received reports of adverse events related to this recall. Recalled Products: These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The recalled products are as follows: Product, Sizes and LOT:
FLORANCE MORRIS Antiseptic Hand Sanitizer
8 fl oz, 1 L
LOT CODES: 200520673, 200520674, 200525677, 200601685 The Hand Sanitizer is packaged in an 8 oz. and 1L plastic clear bottles with flip-top caps. Product was distributed in the state of FLORIDA in the United States through one distributor. Grupo Asimex de Mexico is notifying its distributor by recall letter and consumers via this press release. Grupo Asimex de Mexico is arranging for the return and refund of all recalled products. Consumers/distributors that have the product subject to this recall should stop using/ distributing/ selling the Hand Sanitizer and return it to the place of purchase. Consumers with questions regarding this recall can contact Grupo Asimex de Mexico SA de CV during business hours to the following email: sales@asimexglobal.com Event: Recall Consumers should contact their physician or healthcare provider if they experienced any problems that may be related to the use of 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. 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 updates on hand sanitizers consumers should not use
Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/grupo-asimex-de-mexico-sa-de-cv-issues-voluntary-nationwide-recall-all-lots-florence-morris
Source: FDA
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Company name: Grupo Yacana México S.A.S de C.V.
Brand name: Yacana
Product recalled: Yacana Hand Sanitizer, 70% Alcohol
Reason of the recall: Potential Presence of Methanol (Wood Alcohol) and sub-potent ethanol
FDA Recall date: August 18, 2020
Recall details: Guadalupe, Nuevo León, Grupo Yacana México S.A.S de... See More C.V. is voluntarily recalling All Lots of Yacana Hand Sanitizer, 70% Alcohol, 250 ml to the consumer level. The products have the potential to contain methanol (wood alcohol) and be sub-potent for the ethanol content.

Risk Statement: The use of sub-potent hand sanitizer products can have adverse health consequences related to infections. Ethanol levels below the label claim can result in a lack of efficacy. In addition, methanol has inferior antiseptic properties compared to ethanol. 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 person using these products on their hands are at risk, your 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, Grupo Yacana Mexico S.A. de C.V. has not received any reports of adverse events related to this recall. The product is used as a hand sanitizer to help reduce bacteria in hands and is packaged in 250 ml bottles, All lots (NDC: 76592-001-01) and All lots (NDC: 76592-002-04) The product can be identified by the label attached in this recall.

Hand Sanitizer was distributed Nationwide in the USA to Wholesale distributors. Grupo Yacana México S.A.S de C.V. is notifying its distributors and customers by contacting them by email and sending a letter of Product Recall and is arranging for return of all recalled products. Distributors that have Hand Sanitizer which is being recalled should stop using and return to place of purchase. Consumers with questions regarding this recall can contact Grupo Yacana México S.A.S de C.V. at (956) 609 2888 or calidad@yacana.mx on Monday through Friday from 9 am and 5 pm, CST.

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.

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/grupo-yacana-mexico-sas-de-cv-issues-voluntary-nationwide-recall-all-lots-yacana-hand-sanitizer-due

Source: FDA
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Company name: ALBEK de Mexico S.A. de C.V.
Brand name: Nuuxsan, Modesa, more
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: August 18, 2020
Recall details: SAN JUAN del RIO QUERETARO, Mexico -- ALBEK de Mexico S.A. de C.V. is voluntarily recalling... See More 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. Check the link below to see the full list of recalled products.

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.

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/albek-de-mexico-sa-de-cv-issues-voluntary-nationwide-recall-all-hand-sanitizers-due-potential

Source: FDA
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Company name: SG24 LLC
Brand name: SkinGuard24
Product recalled: All Day Hand Sanitizer
Reason of the recall: Contains Methanol
FDA Recall date: August 15, 2020
Recall details: SG24 LLC is voluntarily recalling the SkinGuard24 – All Day Hand Sanitizer products listed below to the consumer level. These... See More products are being recalled because they 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 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, SG24 LLC. has not received any reports of adverse events related to the products of this recall.

Product Name: SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump
Size: 8 oz (250 mL)
UPC: 7 93573 147125
SKU: 051230024

Product Name: SkinGuard24 – All Day Hand Sanitizer Plastic bottle with Foam Pump
Size: 2.67 oz (70 ml)
UPC: 7 93573 147103
SKU: 051220024

Product Name: SkinGuard24 – All Day Hand Sanitizer Spray Pocket Pen
Size: 10 mL
UPC: 7 93573 14709
SKU: 051210048

Product Name: SkinGuard24 – All Day Hand Sanitizer Individual Towelette packaged as Single Use
Size: n/a
UPC: 2.5 x 3.75
SKU: 03150025

The recalled products are used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The recalled products are packaged in PET or High-density polyethylene (HDPE) plastic bottle or pen and as Individually packaged Towelettes with UPC’s 7935733144725, 79357314703, 7935733147103, 79357314709. The recalled products label colors are teal and blue which includes the words SkinGuard24- All Day Hand Sanitizer. The recalled products were distributed nationwide throughout the United States.

SG24 LLC is notifying its customers/distributors by recall letter and consumers via this press release. We are also notifying our 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 recalled products should stop use or distribution and return to place of purchase. Consumers should contact their physician or healthcare provider if they experience any of the aforementioned problems that may be related to the use of this product.

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sg24-llc-issues-voluntary-nationwide-recall-skinguard24-hand-sanitizer-labeled-contain-methanol

Source: FDA
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Company name: Soluciones Cosmeticas
Brand name: Bersih
Product recalled: Hand Sanitizer Gel
Reason of the recall: Potential Methanol Contamination
FDA Recall date: August 09, 2020
Recall details: Company Announcement Soluciones Cosméticas voluntary recalled all lots of Bersih Hand Sanitizer Gel Fragrance Free sold in 16.9 ounce bottles... See More to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol). This release provides additional information about the packaging for the recalled products. 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 Soluciones Cosméticas has not received reports of adverse events related to this recall. The product is used as a hand sanitizer and is packaged in 16.9 ounce plastic clear bottles with blue tops or green tops with UPC Codes 816822026667 or 7503007103178. The lot numbers range from 0100K01 to 0148K01. This product was distributed nationwide to wholesale distributors and retailers. Soluciones Cosméticas is notifying its distributors by voluntary recall letter and consumers via this press release. Consumers that have the product subject to this recall should stop using and either contact Soluciones Cosméticas per the below for disposal instructions or return it to the place of purchase. Consumers with questions regarding this recall can contact Soluciones Cosméticas at  866-912-8410 Monday through Friday 8am to 5pm Eastern Time or by email at bersihrecall6551@stericycle.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to 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. 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. Original Press Release FDA updates on hand sanitizers consumers should not use.
Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/soluciones-cosmeticas-issues-voluntary-nationwide-recall-bersih-hand-sanitizer-gel-due-potential-0
Source: FDA
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