The Recall Desk
ModerateFDA (Drugs)·D-084-2013·Announced 2012-12-12

Lloyd Inc. Recalls Thyro-Tab 0.300 mg Tablets Due to cGMP Deviations

Lloyd Inc. of Iowa is recalling 1,902,957 Thyro-Tab 0.300 mg tablets because they do not meet in-process specification requirements.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or hospitalizations. The hazard is a manufacturing deviation (cGMP) without reported harm, fitting the Moderate category for low-risk contamination or voluntary precautionary recalls.

Plain-English summary

Lloyd Inc. of Iowa is recalling 1,902,957 tablets of Thyro-Tab 0.300 mg. The product is packaged in 150,000-tablet bulk drums for repackaging and is a prescription (RX) medication. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

The recall was initiated because the product does not meet in-process specification requirements and involves cGMP (Current Good Manufacturing Practice) deviations. The specific nature of the deviations is not detailed in the source text.

Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution. The affected lot number is HE35311. Consumers and healthcare providers should check their inventory for this specific lot and contact their healthcare provider or the recalling firm for instructions on disposal or replacement.

The recalled product

Product
Thyro-Tab 0.300 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.
Manufacturer
Lloyd Inc. of Iowa
Category
Drug — Thyroid Medication
Hazard
Affected units
1,902,957

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot #HE35311

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 12 recalled by Lloyd Inc. of Iowa under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 12 products in this recall →

Related recalls

Same manufacturer · Lloyd Inc. of Iowa

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Same hazard · cGMP deviation

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