Levothroid recall: CGMP Deviations
Levothroid (levothyroxine sodium tablets, USP), 300 mcg., 100-count bottles, Rx only, NDC 0456-1328-01, Manufactured for Forest Pharmaceuticals, Inc.…
Why was Levothroid recalled?
cGMP Deviations; does not meet in process specification requirements
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 #1097178 exp. 7/31/2013
- Product
- Levothroid (levothyroxine sodium tablets, USP), 300 mcg., 100-count bottles, Rx only, NDC 0456-1328-01, Manufactured for Forest Pharmaceuticals, Inc.…
- Recalling firm
- Lloyd Inc. of Iowa
- Quantity
- 1,443/100-tablet bottles
- Distribution
- Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution.
- Recall date
- December 12, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)