FDA Enforcement Class II Ongoing

Medline procedural kits labeled as: 1) PERIPHERAL ULTRASOUND CATHETER INSERTION, Pack Number MNS9865; 2) CIRCUMCISION TRAY, Pack Number CIT6715; 3) OSF SMMC CIRCUMCISION KIT, Pack Number CIT7095

Recall: Z-2742-2024 · Reported September 4, 2024

Enforcement

Recall Number
Z-2742-2024
Event ID
94581
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
MEDLINE INDUSTRIES, LP - Northfield
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
September 4, 2024
Initiation Date
April 8, 2024
Classification Date
August 28, 2024
Address
3 Lakes Dr, Northfield, IL, 60093-2753, United States

Description

Medline procedural kits labeled as: 1) PERIPHERAL ULTRASOUND CATHETER INSERTION, Pack Number MNS9865; 2) CIRCUMCISION TRAY, Pack Number CIT6715; 3) OSF SMMC CIRCUMCISION KIT, Pack Number CIT7095

Reason

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Code Info

1) MNS9865 , Lot Number 2021111050; 2) CIT6715 , Lot Number 2023050590; 3) CIT7095 , Lot Number 2023091990;

Distribution

Worldwide