# FDA recall D-074-2013

> **Lloyd Inc. of Iowa** · Class II · drug recall initiated 2012-07-09.

## Product

Thyro-Tab 0.050 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

## Reason for recall

cGMP Deviations; does not meet in process specification requirements

## Distribution

Distribution was nationwide, including Puerto Rico.  There was no foreign, military, or government distribution.

## Key facts

- **Recall number:** D-074-2013
- **Recalling firm:** Lloyd Inc. of Iowa
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-07-09
- **Report date:** 2012-12-12
- **Termination date:** 2013-11-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Shenandoah, IA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-074-2013

## Citation

> AI Analytics. FDA recall D-074-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-074-2013. Source: US FDA. Licensed CC0.

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