The Recall Desk
ModerateFDA (Drugs)·D-078-2013·Announced 2012-12-12

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

Lloyd Inc. of Iowa is recalling 3.8 million Thyro-Tab 0.112 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 specific high-risk pathogens, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Lloyd Inc. of Iowa is recalling 3,813,645 tablets of Thyro-Tab 0.112 mg. The product is packaged in 150,000-tablet bulk drums intended for repackaging and is available by prescription. The label identifies the firm as 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 or the exact specifications not met are not detailed in the source text.

Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution. The affected lots are #HC31411 and #HE18711. Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider or pharmacist for guidance.

The recalled product

Product
Thyro-Tab 0.112 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 — Prescription Medication
Hazard
Affected units
3,813,645

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 #HC31411 and #HE18711

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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