Severity
Low
LowClass IIIOngoing
FDA Drug recall · Reported November 15, 2023
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
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.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
AbbVie Inc. recalled Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only … - a low-severity action.
Synthroid, Levothyroxine Sodium Tablets, USP 125mcg (0.125mg), 100-count bottle, Rx Only … was recalled by AbbVie Inc. in November 15, 2023. Reason: Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode informa…. Check the official notice for the remedy. Verify recall #D-0088-2024 with the FDA Drug before acting.
The recall
AbbVie Inc. issued this low-severity FDA Drug recall-Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode informa….
- Low
- severity level
- Class III
- classification
- November 15, 2023
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0088-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0088-2024) was formally reported on November 15, 2023, with the manufacturer initiating the action on October 17, 2023. It is classified under Low severity (Class III), with a current status of Ongoing. AbbVie Inc. is listed as the recalling firm, operating out of North Chicago, IL. Federal records list the affected scope as 864 cartons.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Distributed in the US. No government or foreign consignees.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
864 cartons
Related Recalls
6
0 from same agency
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Ongoing |
| Recall number | D-0088-2024 |
| Date reported | November 15, 2023 |
| Date initiated | October 17, 2023 |
| Recalling firm | AbbVie Inc. |
| Firm location | North Chicago, IL |
| Affected scope | 864 cartons |
| Distribution | Distributed in the US. No government or foreign consignees. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0088-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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.
Where was the recalled product distributed? ▼
Distribution: Distributed in the US. No government or foreign consignees..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0088-2024) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported November 15, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.