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