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

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe