Recall Record

Dubuque, IA, United States

The Metrix Company recalls

2 recalls recorded since 2018, most recently on 9 October 2024. 2 are listed as ongoing. Status and classification are as published by the FDA.

Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0

Ongoing Class II Medical devices

Recall started
9 October 2024
Reason
A limited number of IV bags have been found to leak during filling.
Distribution
Worldwide - US Nationwide distribution in the states of TX, IL, OH, PA, WA, MD, IL, UT, CA, MA, PA, MI, FL, PR, and the country of Canada.
Initiated
Voluntary: Firm initiated
Recall numbers
Z-0339-2025, Z-0335-2025, Z-0344-2025, Z-0330-2025, Z-0342-2025, Z-0332-2025, Z-0337-2025, Z-0343-2025, Z-0334-2025, Z-0333-2025, Z-0336-2025, Z-0338-2025 and 4 more

Ongoing Class II Medical devices

Recall started
21 September 2018
Reason
Potential for leaking product
Distribution
US Nationwide distribution including the states of PA, MA, IL CA.
Initiated
Voluntary: Firm initiated
Recall numbers
Z-0003-2020, Z-0004-2020, Z-0005-2020, Z-0008-2020, Z-0001-2020, Z-0007-2020, Z-0006-2020, Z-0002-2020

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.