The Recall Desk
ModerateFDA (Drugs)·D-076-2013·Announced 2012-12-12

Lloyd Inc. Recalls Thyro-Tab 0.088 mg. Tablets Due to cGMP Deviations

Lloyd Inc. of Iowa is recalling 3.8 million Thyro-Tab 0.088 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. The source text does not report any illnesses, injuries, or hospitalizations, and the hazard is related to manufacturing deviations rather than a specific high-risk pathogen or structural defect, fitting the criteria for a moderate severity score.

Plain-English summary

Lloyd Inc. of Iowa is recalling 3,826,269 tablets of Thyro-Tab 0.088 mg. The product is packaged in 150,000-tablet bulk drums intended for repackaging and is available by prescription. 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 Current Good Manufacturing Practice (cGMP) 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 #HA31411 and #HE17811. Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider or the recalling firm for further instructions.

The recalled product

Product
Thyro-Tab 0.088 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
3,826,269

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 #HA31411 and #HE17811

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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