The Recall Desk
ModerateFDA (Drugs)·D-080-2013·Announced 2012-12-12

Lloyd Inc. Recalls Thyro-Tab 0.125 mg. Tablets Due to cGMP Deviations

Lloyd Inc. of Iowa is recalling 1,924,174 tablets of Thyro-Tab 0.125 mg. (Lot #HB27811) because the product does 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 cites cGMP deviations and failure to meet in-process specifications but does not report any illnesses, injuries, or specific high-risk pathogens, aligning with the 'Moderate' severity criteria for minor labeling or process errors without reported harm.

Plain-English summary

Lloyd Inc. of Iowa is recalling 1,924,174 tablets of Thyro-Tab 0.125 mg. (Lot #HB27811). The product is packaged in 150,000-tablet bulk drums intended 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 involves cGMP (Current Good Manufacturing Practice) deviations and does not meet in-process specification requirements. No specific illnesses or injuries are reported in the source text.

Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution. 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 0.125 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
1,924,174

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 #HB27811

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

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Same hazard · cGMP deviation

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