Class II — Potential Health Hazard

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

MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba MOOG Medical Devices Group) Due to Administration sets leaked at the filter.

Date: February 27, 2019
Company: Zevex Incorporated (dba MOOG Medical Devices Group)
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 Zevex Incorporated (dba MOOG Medical Devices Group) directly.

Affected Products

MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.

Quantity: 756/20-set cases

Why Was This Recalled?

Administration sets leaked at the filter.

Where Was This Sold?

This product was distributed to 6 states: GA, IL, KS, MA, MI, OH

Affected (6 states)Not affected

About Zevex Incorporated (dba MOOG Medical Devices Group)

Zevex Incorporated (dba MOOG Medical Devices Group) has 2 total recalls tracked by RecallDetector.

Related Recalls

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