FDAFDA · Food and drugs·Recall number D-0088-2024
Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only AbbVie Inc. North Chicago, IL 60064, U.S.A. NDC 0074-7068-11
Published November 15, 2023 · Recall initiated: October 17, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SYNTHROID
- Manufacturer
- AbbVie Inc.
- Distributor
- Distributed in the US. No government or foreign consignees.
- UPC
- 0300747149902
- Lot
- Lot # 1187435 exp date: 02/2024
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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