FDA Enforcement Class II Terminated

CHS Custom Convenience Kit-LP NEEDLE, 22G X 1 Product Number:NC401000

Recall: Z-0251-2019 · Reported October 31, 2018

Enforcement

Recall Number
Z-0251-2019
Event ID
81179
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Custom Healthcare Systems, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 31, 2018
Initiation Date
August 13, 2018
Classification Date
October 25, 2018
Termination Date
August 1, 2022
Address
4205 Eubank Rd, N/A, Richmond, VA, 23231-4328, United States

Description

CHS Custom Convenience Kit-LP NEEDLE, 22G X 1 Product Number:NC401000

Reason

Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility

Code Info

Lot number: 51018 Exp. Date:5/1/2021

Distribution

Connecticut, Georgia, Kentucky, North Carolina, Virginia, Maryland, Oklahoma, Illinois, South Carolina,

Quantity

250 units