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AbbVie Inc.

AbbVie Inc. Recalls

All product recalls associated with AbbVie Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Sep 2024

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

Refresh P.M. Eye Ointment (AbbVie) – Tube Seal Breach (2024)

Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.

Class IIModerate

FDASep 16, 2024Nationwide• AbbVie Inc.

Refresh LACRI-LUBE (AbbVie) – Tube Seal Breach (2024)

Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.

Class IIModerate

FDASep 16, 2024Nationwide• AbbVie Inc.

Synthroid Levothyroxine Tablets (AbbVie) – Incorrect Barcode (2023)

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.

Class IIILow

FDAOct 17, 2023IN, OR• AbbVie Inc.