FDA Enforcement Class II Terminated

Medtronic CB10W64R1, Custom Pack CB10W64R1 CH Access 3/8, Custom Perfusion System, Sterile, Rx.

Recall: Z-1882-2021 · Reported June 23, 2021

Enforcement

Recall Number
Z-1882-2021
Event ID
87915
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Medtronic Perfusion Systems
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
June 23, 2021
Initiation Date
April 29, 2021
Classification Date
June 16, 2021
Termination Date
March 20, 2023
Address
7611 Northland Dr N, Brooklyn Park, MN, 55428-1088, United States

Description

Medtronic CB10W64R1, Custom Pack CB10W64R1 CH Access 3/8, Custom Perfusion System, Sterile, Rx.

Reason

Specific lots may have been manufactured with insufficient or incomplete welds.

Code Info

GTIN 00763000341015, Lot numbers 221102372, Use By 2022-09-21; and 221672013, Use By 2022-11-02

Distribution

US Nationwide Distribution in the states of AL, AZ, CA, IN, KY, MA, OH, TN, and TX. There was no foreign/government/military distribution.

Quantity

12 tubing packs