FDAFDA · Food and drugs·Recall number D-318-2013
Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by: Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0220-01,
Published May 15, 2013 · Recall initiated: March 12, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications: 3 month stability testing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- L. Perrigo Co.
- Distributor
- Nationwide
- Lot
- 12K714 exp. 12/13, 12K715 exp. 12/13
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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