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DiBAR LABS Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ. (236.5 mL), Distributed by S.E.N.D. LLC, ...

FDA Recall #D-0644-2021 — Class I — May 11, 2021

Recall #D-0644-2021 Date: May 11, 2021 Classification: Class I Status: Terminated

Product Description

DiBAR LABS Hand Sanitizer (ethyl alcohol 70%), 8 FL OZ. (236.5 mL), Distributed by S.E.N.D. LLC, Anthony, NM 88021, Imported by Dibar Labs, LLC, Sugar Land, TX 77479, Made in Mexico,77479, NDC 73009-0001-08 UPC 8 53090 00301 3.

Reason for Recall

Chemical Contamination: FDA analysis found 3 lots of DiBAR hand Sanitizer to be below the label claim for ethanol content and to contain methanol.

Recalling Firm

DIBAR NUTRICIONAL S DE RL DE CV — Morelia, N/A

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

Unknown quantity

Distribution

Distributed Nationwide in the USA

Code Information

Lot # LDHSN050920 T1, LDHSN051020 DESC, LDHSN051020 T2, EXP 05/2022

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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