Class III โ€” Low Risk

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

Vyvanse (lisdexamfetamine dimesylate) Capsules 30 mg Recalled by Shire Due to Presence of Foreign Tablets/Capsules

Date: September 2, 2016
Company: Shire
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 Shire directly.

Affected Products

Vyvanse (lisdexamfetamine dimesylate) Capsules 30 mg, 100 count bottle, Rx Only, Manufactured for: Shire US, Inc., Lexington, MA 02421, NDC 59417-103-10

Quantity: 7,680 bottles (768,000 capsules)

Why Was This Recalled?

Presence of Foreign Tablets/Capsules

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Shire

Shire has 2 total recalls tracked by RecallDetector.

Related Recalls

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