Recall Z-1067-2020— 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- Pathology Container 1150ST STERILE GRADUATED CONTAINER, 32 OZ. 17070 AI OR CARDIAC STERILE KIT 3703ST STERILE PATHOLOGY CONTAINER 3706ST STERILE CONTAINER 165 OZ.. 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- Pathology Container 1150ST STERILE GRADUATED CONTAINER, 32 OZ. 17070 AI OR CARDIAC STERILE KIT 3703ST STERILE PATHOLOGY CONTAINER 3706ST STERILE CONTAINER 165 OZ.

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.