# FDA recall D-1158-2022

> **Walmart Inc** · Class II · drug recall initiated 2022-05-24.

## Product

Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.

## Reason for recall

Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.

## Distribution

Nationwide in the USA.

## Key facts

- **Recall number:** D-1158-2022
- **Recalling firm:** Walmart Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Completed
- **Initiation date:** 2022-05-24
- **Report date:** 2022-06-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bentonville, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1158-2022

## Citation

> AI Analytics. FDA recall D-1158-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1158-2022. Source: US FDA. Licensed CC0.

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