Synthroid
5 FDA drug recalls involving brand “Synthroid”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2023-10-17 | Class III | Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie Inc. North Chi | AbbVie Inc. |
| 2012-12-04 | Class II | Synthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bottle, Rx Only, NDC 0074-7069-90; | Abbott Laboratories |
| 2012-07-19 | Class II | Synthroid (levothyroxine sodium) Tablets USP, 112 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Ch | Abbott Laboratories |
| 2012-07-19 | Class II | Synthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chi | Abbott Laboratories |
| 2012-07-19 | Class II | Synthroid (levothyroxine sodium) Tablets USP, 50 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chi | Abbott Laboratories |