Health product recall

Infusomat® Space Pump IV Set with Anti-Siphon Valve

Last updated

Summary

Product
Infusomat® Space Pump IV Set with Anti-Siphon Valve
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 catalog number

Infusomat® Space Pump IV Set With Anti-Siphon Valve

lot numbers lower than 0061902124

363901
363433
363420
363424
363904
363421
363423
363430
363410

Infusomat® Space Pump Y-Type Blood IV Set With Anti-Siphon Valve

lot numbers lower than 0061902124

363419

Infusomat® Space Pump Low Adsorption IV Set With Anti-Siphon Valve

lot numbers lower than 0061902124

363902

Infusomat® Space Pump Burette IV Set With Anti-Siphon Valve

lot numbers lower than 0061902124

363032
363422

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 23, 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-74606

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