# FDA recall D-0810-2018

> **Aidarex Pharmaceuticals LLC** · Class III · drug recall initiated 2018-04-10.

## Product

Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00

## Reason for recall

Presence of Foreign Tablets/Capsules

## Distribution

Product was distributed to Florida

## Key facts

- **Recall number:** D-0810-2018
- **Recalling firm:** Aidarex Pharmaceuticals LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-04-10
- **Report date:** 2018-05-23
- **Termination date:** 2019-12-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Corona, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0810-2018

## Citation

> AI Analytics. FDA recall D-0810-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0810-2018. Source: US FDA. Licensed CC0.

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