Z-1095-2018 Class II Terminated

Recalled by Centurion Medical Products Corporation — Williamston, MI

FDA device recall Z-1095-2018 was initiated by Centurion Medical Products Corporation on October 23, 2017 and is designated Class II. Reason for recall: Convenience Kit containing components to assist practitioner with IV placement and securement. The recall status is terminated (terminated June 21, 2018). Affected quantity: N/A.

Recall Details

Product Type
Devices
Report Date
March 28, 2018
Initiation Date
October 23, 2017
Termination Date
June 21, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

NEONATAL IV START KIT

Reason for Recall

Convenience Kit containing components to assist practitioner with IV placement and securement.

Distribution Pattern

Nationally

Code Information

IVS425 Lot codes: 2016091290 2016082290