Health product recall

Parapac Plus 310

Last updated

Summary

Product
Parapac Plus 310
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Parapac Plus 310

Not applicable.

P310NCAFREN
P310NCA
P310NUS

Issue

An issue involving a Parapac Plus™ P310 ventilator, where there is potential for inadvertent tidal volume knob movement from the original setting, when set at high (1000 - 1500 ml) and low (70 - 150 ml) settings.

Recall start date: June 5, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies
Smiths Medical Asd, Inc.
6000 Nathan Lane N., Minneapolis, Minnesota, United States, 55442
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75721

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