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CareFusion 303, Inc. recalls VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a
Recalled August 23, 2017 · FDA recall Z-3030-2017 · CareFusion 303
Hazard
Punctures in blister packaging that was detected during the packaging process. · FDA Class II
Units
1,546,800 units
Sold at
Worldwide Distribution in the states of : CO, IL, IN, MD, MI, NY, OH, & TX. and foreign countries of: Australia, New Zealand, & Japan.
Description
Punctures in blister packaging that was detected during the packaging process.
Product
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.
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →