Recall Z-1022-2020— Cardinal Health

Class II · Terminated

Class II FDA medical device recall by Cardinal Health, initiated 2020-01-11, terminated 2023-01-19. It names one FDA 510(k) clearance: K020593. Product: ROYALSILK LARGE, Gown. Item Code 9518. Reason: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination..

Recalling firm
Cardinal Health
Classification
Class II
Status
Terminated
Initiated
2020-01-11
Terminated
2023-01-19
Firm location
Waukegan, IL, United States

510(k) clearances named in this recall

1 on FDA's record

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

ROYALSILK LARGE, Gown. Item Code 9518

Reason for recall

The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.

Data sourced from openFDA. This site is unofficial and independent of the FDA.