PlainRecalls
FDA Devices Moderate Class II Terminated

IV START KIT

Reported: March 28, 2018 Initiated: October 23, 2017 #Z-1093-2018

Product Description

IV START KIT

Reason for Recall

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

Details

Units Affected
N/A
Distribution
Nationally
Location
Williamston, MI

Frequently Asked Questions

What product was recalled?
IV START KIT. Recalled by Centurion Medical Products Corporation. Units affected: N/A.
Why was this product recalled?
Convenience Kit containing components to assist practitioner with IV placement and securement.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 28, 2018. Severity: Moderate. Recall number: Z-1093-2018.