Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Liothyronine Sodium Tablets Recalled by L. Perrigo Co. Due to Failed Impurities/Degradation Specifications: 3 month stability testing.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact L. Perrigo Co. directly.
Affected Products
Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by: Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0220-01,
Quantity: 21,667 bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications: 3 month stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About L. Perrigo Co.
L. Perrigo Co. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report