CareFusion 303, Inc. recalls VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a fem…

Recall date

June 30, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-3030-2017

FDA classification

Class II

Brand / firm

CareFusion 303, Inc.

Sold / distributed

Worldwide Distribution in the states of : CO, IL, IN, MD, MI, NY, OH, & TX. and foreign countries of: Australia, New Zealand, & Japan.

Why it was recalled

Punctures in blister packaging that was detected during the packaging process.

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

What was recalled

VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a female luer lock adapter to administer fluid and medications through a needle or catheter inserted into a patients artery or vein.