Medical device recalls Moderate risk

Carefusion 2200 Inc recalls Thoracentesis/ Paracentesis Kit 10/CS; STERILE;

Recall date
February 23, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1426-2018
FDA classification
Class II
Brand / firm
Carefusion 2200 Inc
Sold / distributed
Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam

Why it was recalled

The integrity of the sterile packaging is potentially compromised.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Thoracentesis/ Paracentesis Kit 10/CS; STERILE;

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