Drug recall D-0088-2024
Product
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
Reason for recall
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.
Lots and codes
Lot # 1187435 exp date: 02/2024
Recall details
- Recalling firm
- AbbVie Inc., North Chicago, IL
- Quantity
- 864 cartons
- Distribution
- Distributed in the US. No government or foreign consignees.
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 17, 2023
Related products
- Synthroid – drug information
- NDC 0074-3727 Synthroid · Levothyroxine Sodium 137 ug/1 · AbbVie Inc.
- NDC 0074-7068 Synthroid · Levothyroxine Sodium 125 ug/1 · AbbVie Inc.
- NDC 0074-4552 Synthroid · Levothyroxine Sodium 50 ug/1 · AbbVie Inc.
- NDC 0074-6624 Synthroid · Levothyroxine Sodium 100 ug/1 · AbbVie Inc.
- NDC 0074-7149 Synthroid · Levothyroxine Sodium 300 ug/1 · AbbVie Inc.
- NDC 0074-6594 Synthroid · Levothyroxine Sodium 88 ug/1 · AbbVie Inc.
- NDC 0074-9296 Synthroid · Levothyroxine Sodium 112 ug/1 · AbbVie Inc.
- NDC 0074-7070 Synthroid · Levothyroxine Sodium 175 ug/1 · AbbVie Inc.
- NDC 0074-7069 Synthroid · Levothyroxine Sodium 150 ug/1 · AbbVie Inc.
- NDC 0074-7148 Synthroid · Levothyroxine Sodium 200 ug/1 · AbbVie Inc.
- NDC 0074-5182 Synthroid · Levothyroxine Sodium 75 ug/1 · AbbVie Inc.
- NDC 0074-4341 Synthroid · Levothyroxine Sodium 25 ug/1 · AbbVie Inc.