FDA-Device2015-01-14Class II
Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)
Centurion Medical Products Corporation
Hazard
According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
Sold states
Nationwide Distribution including MA, IN, NY, GA, AL, PA, and RI.
Affected count
42 kits
Manufactured in
100 Centurion Way, N/A, Williamston, MI, United States
Products
Chest Tube Tray (Cardiovascular Surgical Instruments convenience kit)
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0942-2015Don't want to check this manually?
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