Class II — Potential Health Hazard

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

AbbVie PEG Recalled by AbbVie Inc. Due to

Date: April 27, 2017
Company: AbbVie Inc.
Status: Terminated
Source: FDA (Device)

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

AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

Quantity: 673 kits

Why Was This Recalled?

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About AbbVie Inc.

AbbVie Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

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