Health product recall

Perfusor® Space® Syringe Pump

Last updated

Summary

Product
Perfusor® Space® Syringe Pump
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Space Infusion System - Perfusor® Space® Infusion Syringe Pump

More than 10 numbers, contact manufacturer.

8713030U
8713031U

Space Infusion System - PCA-Kit

More than 10 numbers, contact manufacturer.

8713080U

Space Infusion System - Perfusor® Space® ACM Pump

More than 10 numbers, contact manufacturer.

8713040U

Perfusor® Space®

More than 10 numbers, contact manufacturer.

8713030C
8713032U

Issue

Cardinal Health began distributing Monoject™ syringes branded as "Cardinal Health Monoject™ syringes" however, the new syringes have different dimensions than prior Covidien Monoject™ syringes. The dimensional changes made to the Cardinal Health Monoject™ syringes, when used with syringe pumps, may result in recognition, compatibility, and pump performance issues, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. The Perfusor® space syringe pump IFU's identify Monoject™ syringes as an option for use with the pumps.

Recall start date: June 4, 2024

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 Melsungen AG

Carl-Braun-Str. 1, Melsungen, Germany, 34212

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75684

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