The Recall Desk
ModerateFDA (Drugs)·D-435-2013·Announced 2013-05-29

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

Lloyd Inc. of Iowa is recalling 9.5 million Thyro-Tab tablets due to cGMP deviations and insufficient stability data.

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, but the source text does not report any illnesses, injuries, or hospitalizations. The hazard is based on cGMP deviations and insufficient stability data, fitting the criteria for a moderate severity score.

Plain-English summary

Lloyd Inc. of Iowa is recalling 9,545,718 tablets of Lloyd Thyro-Tab 0.075 mg. The product was packaged in 150,000-tablet bulk drums for repackaging and is a prescription medication. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

The recall is being conducted due to current Good Manufacturing Practice (cGMP) deviations. Following a quality review of stability failures in previous lots, the firm determined there is insufficient data to confirm that other lots are not affected. The affected lots include HC04712 (Exp. Mar-13), HD08112 (Exp. Apr-13), HE08112, and HD11112 (Exp. May-13).

The bulk product was distributed to Forest Laboratories, Inc. in St. Louis, MO, which repackaged the product into 100-tablet bottles. These bottles were distributed to 75 customers nationwide and in Puerto Rico. Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider or pharmacist for guidance on alternative treatment.

The recalled product

Product
Lloyd Thyro-Tab 0.075 mg., packaged in 150,000-tablet bulk drums (2/75,000-tablet bags/drum) 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
9,545,718

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 (7)

  • Lot #: HC04712
  • Exp. Mar-13
  • HD08112
  • Exp. Apr-13
  • HE08112
  • HD11112
  • Exp May-13.

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 20 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 20 products in this recall →

Related recalls

Same manufacturer · Lloyd Inc. of Iowa

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Same hazard · cGMP deviation

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