Z-1043-2020 Class II Terminated
FDA device recall Z-1043-2020 was initiated by Centurion Medical Products Corporation on December 11, 2019 and is designated Class II. Reason for recall: Incomplete seals on the sterile package may compromise the sterility The recall status is terminated (terminated September 4, 2020). Affected quantity: 448.
Recall Details
- Product Type
- Devices
- Report Date
- February 12, 2020
- Initiation Date
- December 11, 2019
- Termination Date
- September 4, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 448
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
Distribution Pattern
Nationwide Foreign: GHANA
Code Information
Kit Code Product Lot Number CHT1170 CHEST TUBE TRAY 2019011690 CHT1700 CHEST TUBE INSERTION TRAY 2018111490 CHT1760 CHEST TRAY 2019031490 CHT275 CHEST TUBE INSERTION TRAY 2019050890 CHT440 CHEST TUBE INSERTION TRAY 2019050690 CHT701 CHEST TUBE INSERTION TRAY 2019012590 CHT760 CHEST TUBE INSERTION TRAY 2018110890 CHT940 CHEST TUBE INSERTION TRAY 2019010290