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FDAFDA · Food and drugs·Recall number Z-0163-2022

Pneupac paraPac plus 300 ventilator kit, REF P300NGB

Published November 3, 2021 · Recall initiated: July 15, 2021

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

Two devices were labeled with the same serial number

What to do

Voluntary: Firm initiated

Recall details

Manufacturer
Smiths Medical ASD Inc.
Distributor
UK
Lot
SN RF70121
Risk classification
Class III
Area (FDA)
device
Country
United States

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