Levothyroxine Sodium Tablets recall: Subpotent
Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617…
Why was Levothyroxine Sodium Tablets recalled?
Subpotent Drug: Assay below the approved specification
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 #D2300042, Exp Date: 12/31/2025
- Product
- Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617…
- Recalling firm
- ACCORD HEALTHCARE, INC.
- Quantity
- 2,344 bottles
- Distribution
- Nationwide in the USA
- Recall date
- July 23, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)