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.

CREON (pancrelipase) Delayed-Release Capsules Recalled by AbbVie Inc Due to Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon...

Date: September 15, 2014
Company: AbbVie 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 AbbVie Inc directly.

Affected Products

CREON (pancrelipase) Delayed-Release Capsules, Lipase 24,000 USP Units, 250 Capsule Bottles, Rx Only. Marketed by: AbbVie Inc., North Chicago, IL 60064, Product of Germany. NDC 0032-1224-07.

Quantity: 18,021 Bottles

Why Was This Recalled?

Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About AbbVie Inc

AbbVie Inc has 6 total recalls tracked by RecallDetector.

Related Recalls

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