FDA-Device2013-12-11Class II
VersaSafe Extension Set, Model No. 21000M-007
CareFusion 303, Inc.
Hazard
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
Sold states
Nationwide Distribution.
Affected count
3500 units
Manufactured in
10020 Pacific Mesa Blvd, N/A, San Diego, CA, United States
Products
VersaSafe Extension Set, Model No. 21000M-007
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0435-2014Don't want to check this manually?
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