# FDA recall D-0659-2021

> **Sanit Technologies, LLC dba Durisan** · Class II · drug recall initiated 2021-03-10.

## Product

Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, packaged in 80-count canister (UPC 8 52379 00632 5), b) 160-count canister (UPC 8 52379 00631 8), and c) 240-count canister (UPC 8 52379 00633 2); Sanit Technologies, LLC, 7810 25th Court East, Sarasota, Florida 34243.

## Reason for recall

CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.

## Distribution

Nationwide in the USA and Bahamas

## Key facts

- **Recall number:** D-0659-2021
- **Recalling firm:** Sanit Technologies, LLC dba Durisan
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-03-10
- **Report date:** 2021-07-21
- **Termination date:** 2022-01-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sarasota, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0659-2021

## Citation

> AI Analytics. FDA recall D-0659-2021. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/D-0659-2021. Source: US FDA. Licensed CC0.

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