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
Reported: November 15, 2023 Initiated: October 17, 2023 #D-0088-2024
Product Description
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.
Details
- Recalling Firm
- AbbVie Inc.
- Units Affected
- 864 cartons
- Distribution
- Distributed in the US. No government or foreign consignees.
- Location
- North Chicago, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by AbbVie Inc.. Units affected: 864 cartons.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 15, 2023. Severity: Low. Recall number: D-0088-2024.
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