Recall of Eliquis® (apixaban) 5 mg Tablets

On June 10, Bristol-Myers Squibb announced a voluntary recall of one lot (#HN0063) of Eliquis5 mg tablets. This lot was distributed nationwide in the U.S. to wholesalers and retail pharmacies in February 2017. Bristol-Myers Squibb is taking this precautionary measure based on a single customer complaint that a bottle labeled as Eliquis5 mg was found to contain Eliquis 2.5 mg tablets. No other lots are impacted by this recall.
This recall is to the retail/dispensing level and not to the consumer level. This recall is under way and is currently being executed. The recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Patients shouldnot stop taking Eliquiswithout consulting with their physician.
Please see Eliquis U.S. Full Prescribing Information, including Boxed WARNINGS.
For any customer or patient questions, please call:

General and Medical Inquiries Bristol-Myers Squibb Customer Information Center
Recall Logistics FedEx Supply Chain
Reimbursement/Replacement Process FedEx Supply Chain

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Additional Bristol-Myers Squibb Contacts:
Media: Ken Dominski, 609-252-5251, [email protected]
Investors: Tim Power 609-252-7509, [email protected]
Previous related recall: Bristol-Myers Squibb Voluntarily Recalls One Lot of Eliquis (apixaban) 5 mg Tablets

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