Class II · ModerateRecall completed
Levoxyl
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #:18A18, Exp. 01/2020
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Superpotent Drug.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byPfizer Laboratories Div Pfizer Inc
| Brand name | LEVOXYL |
| Generic name | LEVOTHYROXINE SODIUM |
| Active ingredient(s) | LEVOTHYROXINE SODIUM |
| Distributed by / for | Pfizer Inc. New York, NY 10017 |
| NDC | 60793-855-01 |
Show the full FDA record
| Full product label | Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx Only,Distributed by Pfizer Inc. New York, NY 10017, NDC 60793-855-01 |
| Recalling firm | Pfizer Inc. |
| Distribution | Nationwide within the United States |
| Quantity | 1996 bottles |
| Recall initiated | 2018-12-06 |
| Report date | 2018-12-26 |
| Recall completed | 2020-10-08 |
| Recall number | D-0339-2019 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | New York NY United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.