- Firm Announcement Date:
- FDA Publish Date:
- Product Kind:
- Motive for Announcement:
Recall Motive Description
Potential presence of methanol (wooden alcohol)
- Firm Title:
- UVT, INC.
- Model Title:
- Product Description:
Superior Hand Sanitizer, 70% alcohol content material
UVT, INC. is voluntarily recalling 38,830 liters of SANIDERM ADVANCED HAND SANITIZER, packaged in 1-liter bottles to the patron stage. The merchandise are being recalled because of the 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 injury to the nervous system or loss of life. Though all individuals utilizing these merchandise on their palms 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. To this point, UVT, INC. has not obtained any reviews of antagonistic 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 consists of lot quantity 0530, Expiration date 04/2022. The product might be recognized by the label beneath. Product was distributed Nationwide in the USA.
UVT, INC. is notifying its distributors and clients by cellphone 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 stage, and return all merchandise to the place of buy. buy.
Customers with questions concerning this recall can contact UVT, INC. by cellphone (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.
Adversarial reactions or high quality issues skilled with the usage of this product could also be reported to the FDA’s MedWatch Adversarial 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 kind, then full and return to the tackle on the pre-addressed kind, or submit by fax to 1-800-FDA-0178
This recall is being performed with the information of the U.S. Meals and Drug Administration.
Firm Contact Info