FDA recall D-318-2013

L. Perrigo Co. · Class III · drug

Product

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

Reason for recall

Failed Impurities/Degradation Specifications: 3 month stability testing.

Distribution

Nationwide

Key facts

Status: Terminated
Initiation date: 2013-03-12
Report date: 2013-05-15
Termination date: 2013-07-24
Voluntary/Mandated: Voluntary: Firm initiated
Location: Allegan, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-318-2013