Class II — Potential Health Hazard

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

CORFLO Recalled by CORPAK MedSystems, Inc. Due to Firm is initiating voluntary correction of CORFLO PEG...

Date: February 3, 2017
Company: CORPAK MedSystems, 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 CORPAK MedSystems, Inc. directly.

Affected Products

CORFLO, PEG Adaptor Repair Kit with ENFit Connectors, Size: 16FR; Product Usage: CORFLO PEG Tubes are intended for delivery of enteral nutrition, water and medications into the stomach. The PEG adapter is the connection point between the tubing and the feeding set/syringe. The adapter is designed as a replaceable component.

Quantity: 2 cases (5 units per case)

Why Was This Recalled?

Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.

Where Was This Sold?

This product was distributed to 3 states: CA, NH, VT

Affected (3 states)Not affected

About CORPAK MedSystems, Inc.

CORPAK MedSystems, Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

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