# FDA recall D-104-2013

> **Alara Pharmaceutical Co** · Class II · drug recall initiated 2012-10-29.

## Product

Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR

## Reason for recall

Subpotent; 15 month stability

## Distribution

Nationwide

## Key facts

- **Recall number:** D-104-2013
- **Recalling firm:** Alara Pharmaceutical Co
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-10-29
- **Report date:** 2013-01-02
- **Termination date:** 2014-01-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Juan, PR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-104-2013

## Citation

> AI Analytics. FDA recall D-104-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-104-2013. Source: US FDA. Licensed CC0.

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