FDA Drug Recalls

Recalls / Class II

Class IID-078-2013

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.

Affected lot / code info
Lot #HC31411 and #HE18711

Why it was recalled

cGMP Deviations; does not meet in process specification requirements

Recalling firm

Firm
Lloyd Inc. of Iowa
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
604 W Thomas Ave, N/A, Shenandoah, Iowa 51601-1744

Distribution

Quantity
3,813,645 tablets
Distribution pattern
Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution.

Timeline

Recall initiated
2012-07-09
FDA classified
2012-12-03
Posted by FDA
2012-12-12
Terminated
2013-11-14
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-078-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.