# FDA recall D-0645-2021

> **DIBAR NUTRICIONAL S DE RL DE CV** · Class II · drug recall initiated 2021-05-11.

## Product

DiBAR LABS Hand Sanitizer, (ethyl alcohol 70%), packaged as a) 16 FL OZ (473.1 mL) bottle, NDC 73009-001-16, UPC 8 53090 00302 0 and b) 8 FL OZ (236.5 mL) bottle, NDC 73009-0001-08, UPC 8 53090 00301 3; Distributed by: S.E.N.D, LLC., Anthony, NM  88021; Imported by: Dibar Labs, LLC., Sugar Land, TX  77479, Made in Mexico.

## Reason for recall

CGMP Deviations: Other lots and products of hand sanitizer recalled because they were manufactured under the same conditions as the product lots found to contain methanol.

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-0645-2021
- **Recalling firm:** DIBAR NUTRICIONAL S DE RL DE CV
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-05-11
- **Report date:** 2021-07-07
- **Termination date:** 2023-03-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morelia, N/A, Mexico

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0645-2021

## Citation

> AI Analytics. FDA recall D-0645-2021. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/D-0645-2021. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
