Recall Z-1421-2018— Carefusion 2200 Inc

Name: FDA recall Z-1421-2018
Creator: U.S. Food and Drug Administration
Published: 2017-02-23

Class II · Terminated

Class II FDA medical device recall by Carefusion 2200 Inc, initiated 2017-02-23, terminated 2019-07-09. FDA's recall record names no specific 510(k) clearance for this event. Product: Manometer, 550 ml three-Way Stopcock; STERILE;. Reason: The integrity of the sterile packaging is potentially compromised..

Recalling firm: Carefusion 2200 Inc
Classification: Class II
Status: Terminated
Initiated: 2017-02-23
Terminated: 2019-07-09
Firm location: Vernon Hills, IL, United States

Product description

Manometer, 550 ml three-Way Stopcock; STERILE;

Reason for recall

The integrity of the sterile packaging is potentially compromised.

Data sourced from openFDA. This site is unofficial and independent of the FDA.