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FDAFDA · Food and drugs·Recall number Z-0061-2021

Kit Model #65021652, MTO Left Heart Kit United Reg Health - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any combination of devices from the NAMIC Fluid Management finished good product families and potentially other devices designed and manufactured by original equipment manufacturers (OEM).

Published October 14, 2020 · Recall initiated: September 14, 2020

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Medline Industries Inc
Distributor
US Nationwide distribution including in the states of CA, CO, CT, OH, TX, and NY.
Lot
Lot 5574586, Exp 01/31/2023
Risk classification
Class II
Area (FDA)
device
Country
United States

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