AbbVie recalls 100-count Synthroid tablets with incorrect barcode that may cause 125mcg dose to be scanned as 200mcg. Affected units are from lot #1187435 expiring 02/2024.
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.
AbbVie is recalling 100-count Synthroid tablets that may have a barcode error causing the 125mcg dose to be scanned as 200mcg. This could lead to incorrect medication dosing if the tablets are scanned by pharmacy systems.
The barcode error means a 125mcg tablet may be scanned as 200mcg by pharmacy systems. This could result in receiving a higher dose than intended, potentially causing overmedication.
People with a prescription for Synthroid tablets from AbbVie. Those using the tablets at pharmacies or healthcare facilities that scan barcodes may be affected.
Check for the product name 'Synthroid', 125mcg tablets, 100-count bottle, and lot number 1187435 (expiring 02/2024). The product is sold under NDC 0074-7068-11.
Verify the lot number and expiration date on the packaging to confirm if it matches lot #1187435 expiring 02/2024.
No, the hazard is only in scanning by pharmacy systems. If the tablet is taken as prescribed without scanning, it is safe.
The product has a specific lot number (1187435) expiring 02/2024. Check the packaging for this detail to confirm if it's affected.
No, the remedy is not specified in the recall notice. You can continue using them as long as you check the lot number and expiration date.
We’ve drafted a message you can send AbbVie to request your refund or repair — edit it as you like.
Subject: Recall D-0088-2024 — AbbVie AbbVie Hello, I own a AbbVie that is covered by recall D-0088-2024 from AbbVie. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
