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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug

Lloyd Inc. of Iowa: cGMP Deviations; does not meet in process specification requirements

Agency Publication Date: December 3, 2012
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Affected Products

Product: Thyro-Tab 0.050 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lot #HB01212

Lot Numbers:
HB01212
Product: Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lot #1097830 exp. 1/31/2013

Lot Numbers:
1097830
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.

Lot #HA31411 and #HE17811

Lot Numbers:
HA31411
Product: Levothroid (levothyroxine sodium tablets, USP), 88 mcg., 100-count bottles, Rx only, NDC 0456-1329-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lot #1096369, exp. 11/30/2012; and #1092046, exp. 7/31/2012

Lot Numbers:
1096369
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.

Lot #HC31411 and #HE18711

Lot Numbers:
HC31411
Product: Levothroid (levothyroxine sodium tablets, USP), 112 mcg., 100-count bottles, Rx only, NDC 0456-1330-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lot #1096371, exp. 5/312013; and #1092299, exp. 1/31/2013

Lot Numbers:
1096371
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.

Lot #HB27811

Lot Numbers:
HB27811
Product: Levothroid (levothyroxine sodium tablets, USP),125 mcg., 100-count bottles, Rx only, NDC 0456-1324-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lot #1095210, exp. 4/30/2013

Lot Numbers:
1095210
Product: Thyro-Tab 0.137 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lot #HA27911 and #HA12511

Lot Numbers:
HA27911
Product: Levothroid (levothyroxine sodium tablets, USP), 137 mcg., 100-count bottles, Rx only, NDC 0456-1331-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lot #1095212 exp. 4/30/2013; and #1088877, exp. 11/30/2012

Lot Numbers:
1095212
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.

Lot #HE35311

Lot Numbers:
HE35311
Product: Levothroid (levothyroxine sodium tablets, USP), 300 mcg., 100-count bottles, Rx only, NDC 0456-1328-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lot #1097178 exp. 7/31/2013

Lot Numbers:
1097178

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 62511
Status: Resolved
Manufacturer: Lloyd Inc. of Iowa
Manufactured In: United States
Units Affected: 12 products (1,923,887 tablets; 13,692/100-tablet bottles; 3,826,269 tablets; 31,252/100-tablet bottles; 3,813,645 tablets; 37,827/100-tablet bottles; 1,924,174 tablets; 19,162/100-tablet bottles; 3,774,541 tablets; 36,978/100-tablet bottles; 1,902,957 tablets; 1,443/100-tablet bottles)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.