Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

BELVIQ¿ (Lorcaserin HCl) Tablets Recalled by Eisai Inc Due to Labeling:Missing Label: Bottles may not have a product...

Date: December 5, 2014
Company: Eisai Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Eisai Inc directly.

Affected Products

BELVIQ¿ (Lorcaserin HCl) Tablets, 10 mg, 60-count bottle, Rx only, Manufactured by: Arena Pharmaceuticals, GmbH, Zofingen, Switzerland, Distributed by: Elsai Inc., Woodcliff, NJ 07677 NDC 62856-52960.

Quantity: 121,680 bottles

Why Was This Recalled?

Labeling:Missing Label: Bottles may not have a product label, or have a label with missing or illegible lot number and/or expiry date.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Eisai Inc

Eisai Inc has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report