Class II — Potential Health Hazard

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

Dual Chamber Container fill with gravity/attached transfer sets Recalled by The Metrix Company Due to An issue was identified after a redesign of...

Date: June 23, 2016
Company: The Metrix Company
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 The Metrix Company directly.

Affected Products

Dual Chamber Container fill with gravity/attached transfer sets, 250 mL / 1250 mL, 300 mL / 1700 mL, 500 mL / 2500 mL, 500 mL / 3500 mL

Quantity: 18,474 case

Why Was This Recalled?

An issue was identified after a redesign of the auto compounding device. The compounder cannot meet the designed accuracy specification when dispensing into bags. After reviewing the initial design of the device, it was determined the dispensing volume validation was not properly done and none of the compounders on the market can meet the stated specifications.

Where Was This Sold?

This product was distributed to 20 states: AL, AZ, CA, CO, CT, FL, IL, IA, KS, LA, MD, MA, MN, NC, OH, PA, TN, TX, UT, WA

Affected (20 states)Not affected

About The Metrix Company

The Metrix Company has 33 total recalls tracked by RecallDetector.

Related Recalls

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