# FDA recall D-0662-2021

> **Ummzy, LLC** · Class I · drug recall initiated 2021-03-30.

## Product

Krazy Night capsule, packaged in a) 1-count per blister card and b) 10-count boxes, Manufactured by: SUM MARKETING LLC, Made in USA UPC 746695241860

## Reason for recall

Marketed Without An Approved NDA/ANDA: Products found to contain undeclared tadalafil and/ or sildenafil and vardenafil making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.

## Distribution

USA Nationwide

## Key facts

- **Recall number:** D-0662-2021
- **Recalling firm:** Ummzy, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-03-30
- **Report date:** 2021-07-28
- **Termination date:** 2022-06-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Palisades Park, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0662-2021

## Citation

> AI Analytics. FDA recall D-0662-2021. Retrieved 2026-08-17 from https://api.ai-analytics.org/recall/D-0662-2021. Source: US FDA. Licensed CC0.

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