# FDA recall D-1463-2022

> **Midlab Incorporated** · Class II · drug recall initiated 2022-08-08.

## Product

Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303

## Reason for recall

CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

## Distribution

Naionwide within the United States

## Key facts

- **Recall number:** D-1463-2022
- **Recalling firm:** Midlab Incorporated
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-08-08
- **Report date:** 2022-08-31
- **Termination date:** 2023-08-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Athens, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1463-2022

## Citation

> AI Analytics. FDA recall D-1463-2022. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/D-1463-2022. Source: US FDA. Licensed CC0.

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