US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 12, 2013 (13 years ago)

Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation Specifications: 3 month stability testing.

What was recalled

Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by: Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0220-01,

Recalling firm
L. Perrigo Co.
NDC code
0574-0220-01
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-318-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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