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
Reported: April 19, 2023 Initiated: March 8, 2023 #D-0532-2023
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
Reason for Recall
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.
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 1,926 Bottles
- Distribution
- Nationwide in the USA
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Pfizer Inc.. Units affected: 1,926 Bottles.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 19, 2023. Severity: Low. Recall number: D-0532-2023.
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