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.

Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due to Defective Delivery System; reports of damaged product that...

Date: August 24, 2016
Company: Sandoz 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 Sandoz Inc directly.

Affected Products

Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 24 patches Multi pack, Rx only, Marketed by Baxter Healthcare Cop/Novartis, Deerfield, IL 60015, Manufactured by:Alza Corporation, Vacaville, CA 95688 for Novartis Consumer Health Inc., Parsippany, NJ 07054

Quantity: 42,740 cartons (24 count carton from 7 total lots)

Why Was This Recalled?

Defective Delivery System; reports of damaged product that may alter the predicted release of scopolamine following transdermal application.

Where Was This Sold?

This product was distributed to 1 state: TN

Affected (1 state)Not affected

About Sandoz Inc

Sandoz Inc has 30 total recalls tracked by RecallDetector.

Related Recalls

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