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Saniderm Advanced Hand sanitizer Recall

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Saniderm Advanced Hand sanitizer Recall

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The product was distributed Nationwide in america.


UVT, INC. is voluntarily recalling 38,830 liters of SANIDERM ADVANCED HAND SANITIZER, packaged in 1-liter bottles to the patron degree. The merchandise are being recalled as a result of potential presence of methanol (wooden alcohol)

Danger Assertion: Substantial methanol publicity may end up in nausea, vomiting, headache, blurred imaginative and prescient, everlasting blindness, seizures, coma, everlasting harm to the nervous system or demise. Though all individuals utilizing these merchandise on their fingers are in danger, younger kids who accidently ingest these merchandise and adolescents and adults who drink these merchandise as an alcohol (ethanol) substitute, are most in danger for methanol poisoning. Thus far, UVT, INC. has not obtained any studies of opposed occasions associated to this recall.

The product is used as a hand sanitizer and is packaged in 1-liter plastic bottles. The affected SANIDERM ADVANCED HAND SANITIZER contains lot quantity 0530, Expiration date 04/2022. The product may be recognized by the label (pictured).

The product was distributed Nationwide in america.

UVT, INC. is notifying its distributors and clients by telephone calls, emails and letter and is arranging for substitute and destruction of all recalled merchandise.

Customers/distributors/retailers which have product which is being recalled ought to cease utilizing merchandise, provoke remembers to the person degree, and return all merchandise to the place of buy.

Customers with questions concerning this recall can contact UVT, INC. by telephone (951) 427- 3108 or e-mail to [email protected] Monday to Friday from 9:00 am and three:00 pm Pacific Time. Customers ought to contact their doctor or healthcare supplier if they’ve skilled any issues which may be associated to taking or utilizing this drug product.

Antagonistic reactions or high quality issues skilled with using this product could also be reported to the FDA’s MedWatch Antagonistic Occasion Reporting program both on-line, by common mail or by fax.

  • Full and submit the report Online
  • Common Mail or Fax: Download form or name 1- 800-332-1088 to request a reporting type, then full and return to the deal with on the pre-addressed type, or submit by fax to 1-800-FDA-0178

This recall is being carried out with the data of the U.S. Meals and Drug Administration.

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