Class III โ€” Low Risk

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

Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed...

Date: August 19, 2016
Company: Unichem Pharmaceuticals Usa 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 Unichem Pharmaceuticals Usa Inc directly.

Affected Products

Lamotrigine Tablets, USP, 150 mg, 500-count Tablets per bottle, Rx only, Manufactured by: Unichem Laboratories LTD., Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511 India; Marketed by: Unichem Pharmaceuticals (USA), Inc ., Rochelle Park, NJ 07662; NDC 29300-113-05.

Quantity: 368 bottles

Why Was This Recalled?

Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the tablets.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Unichem Pharmaceuticals Usa Inc

Unichem Pharmaceuticals Usa Inc has 4 total recalls tracked by RecallDetector.

Related Recalls

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