Recall Z-1079-2020— Centurion Medical Products Corporation

Class II · Terminated

Class II FDA medical device recall by Centurion Medical Products Corporation, initiated 2019-12-11, terminated 2020-09-04. FDA's recall record names no specific 510(k) clearance for this event. Product: Centurion-Pitcher Kit GR100150ST GRADUATED PITCHER STERILE 1000 CC Y 2018121090 GR1200ST STERILE 1200CC PITCHER KIT Y 2019031990. Reason: Incomplete seals on the sterile package may compromise the sterility.

Recalling firm
Centurion Medical Products Corporation
Classification
Class II
Status
Terminated
Initiated
2019-12-11
Terminated
2020-09-04
Firm location
Williamston, MI, United States

Product description

Centurion-Pitcher Kit GR100150ST GRADUATED PITCHER STERILE 1000 CC Y 2018121090 GR1200ST STERILE 1200CC PITCHER KIT Y 2019031990

Reason for recall

Incomplete seals on the sterile package may compromise the sterility

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