Health product recall

Infusomat® Administration Sets

Last updated

Summary

Product
Infusomat® Administration Sets
Issue
Medical devices - Device compatibility
What to do

Contact the manufacturer if you require additional information. 

Affected products

Affected products

Lot or serial number

Model or catalogue number

Infusomat® Administration Sets

More than 10 numbers, contact manufacturer.

362033
362035
362050
362432
362911
363032
363410
363419
363420
363421
363422
363423
363424
363430
363433
363901
363902
363904
470119
490037
490038
490100
490101
490102
490103
490104
490105

Issue

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit within the Infusomat space pump. If the tubing is stretched or the tubing outer diameter is too small, this may result in suboptimal coupling between the administration set and the air-in-line sensor dampening the signal of the air-in-line sensor. If the signal is dampened, the Infusomat space pump may generate false air-in-line alarms.

Recall start date: October 24, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
B. Braun Medical Inc.
824 12th Avenue, Bethlehem, Pennsylvania, United States, 18018
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-74553

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