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.

Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due to Labeling: Label mix-up. Amitiza 8 mcg capsules are...

Date: May 13, 2019
Company: MALLINCKRODT PHARMACEUTICALS
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 MALLINCKRODT PHARMACEUTICALS directly.

Affected Products

Amitiza (lubiprostone) capsules, 24 mcg, 60-count bottle, Rx only, Manufactured by: Sucampo Pharma Americas, LLC, NDC 64764-240-60

Quantity: 80,640 bottles

Why Was This Recalled?

Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24 mcg capsules were found in a 8 mcg trade 60 ct. bottle. Amitiza 24 mcg capsules are being recalled because a sealed 60 ct. bottle contained only 8 mcg capsules, this incident is being considered as a labeling mix-up issue.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About MALLINCKRODT PHARMACEUTICALS

MALLINCKRODT PHARMACEUTICALS has 2 total recalls tracked by RecallDetector.

Related Recalls

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