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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