Recall Z-1043-2020— 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 Chest Tube Trays: Kit Code Product CHT1170 CHEST TUBE TRAY CHT1700 CHEST TUBE INSERTION TRAY CHT1760 CHEST TRAY CHT275 CHEST TUBE INSERTION TRAY CHT440 CHEST TUBE INSERTION TRAY CHT701 CHEST TUBE INSERTION TRAY CHT760 CHEST TUBE INSERTION TRAY CHT940 CHEST TUBE INSERTION TRAY. 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 Chest Tube Trays: Kit Code Product CHT1170 CHEST TUBE TRAY CHT1700 CHEST TUBE INSERTION TRAY CHT1760 CHEST TRAY CHT275 CHEST TUBE INSERTION TRAY CHT440 CHEST TUBE INSERTION TRAY CHT701 CHEST TUBE INSERTION TRAY CHT760 CHEST TUBE INSERTION TRAY CHT940 CHEST TUBE INSERTION TRAY

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.