Recalls / Class II
Class IID-084-2013
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.
- Affected lot / code info
- Lot #HE35311
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
- 1,902,957 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-084-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.