Thyro-Tab 0.050 mg recall: Subpotent
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.
Why was Thyro-Tab 0.050 mg recalled?
Subpotent; 9-month stability interval
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot HB23111 and HC23111
- 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.
- Recalling firm
- Lloyd Inc. of Iowa
- Quantity
- 3,789,426/50-mcg. tablets
- Distribution
- Distribution was nationwide and to Puerto Rico. There was no foreign, military, or government distribution.
- Recall date
- January 2, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)