Z-1086-2020 Class II Terminated

Recalled by Centurion Medical Products Corporation — Williamston, MI

FDA device recall Z-1086-2020 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: 160.

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
160

Product Description

Centurion- LC145 STERILE NICU LINE CHANGE KIT

Reason for Recall

Incomplete seals on the sterile package may compromise the sterility

Distribution Pattern

Nationwide Foreign: GHANA

Code Information

Lot Code: 2018111590