FDA-Device2013-11-13Class II
Dual Luer Lock Cap The device is intended for use as a cap for male or female Luer ports on medical devices such as manifolds, stopcocks or sets.
Baxter Healthcare Corp.
Hazard
The firm is recalling lots 10043 and 10044 due to loose particulate matter found in the packaging. Particulate matter entering the fluid path from the Luer lock caps may result in embolic events.
Sold states
Worldwide Distribution - USA (nationwide) and the country of Canada.
Affected count
628,992 units
Manufactured in
1 Baxter Pkwy, N/A, Deerfield, IL, United States
Products
Dual Luer Lock Cap The device is intended for use as a cap for male or female Luer ports on medical devices such as manifolds, stopcocks or sets.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0143-2014Don't want to check this manually?
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