FDA recall record

MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle recall — FDA D-0532-2023

Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is…

Class IIIclassification
D-0532-2023official record ID
Apr 19, 2023report date

Recall record at a glance

Official recordD-0532-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmPfizer Inc.
Report dateApr 19, 2023
Recall initiation dateMar 8, 2023
Quantity1,926 Bottles
LocationNew York, NY, United States

Official product description

MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma Inc., a wholly owned subsidiary of Pfizer Inc., Boulder, CO 80301. NDC: 70255-010-02

Why the product was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is February 2025.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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