Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

tabcin NOCHE Recalled by Profarma Distributors LLC Due to CGMP Deviations

Date: May 11, 2016
Company: Profarma Distributors LLC
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 Profarma Distributors LLC directly.

Affected Products

tabcin NOCHE; Capsules,12-count box, UPC 501008485033

Quantity: 31 boxes ( 372 capsules)

Why Was This Recalled?

CGMP Deviations

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Profarma Distributors LLC

Profarma Distributors LLC has 5 total recalls tracked by RecallDetector.

Related Recalls

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