PlainRecalls
FDA Devices Critical Class I Terminated

B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032

Reported: October 2, 2019 Initiated: May 1, 2019 #Z-2489-2019

Product Description

B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032

Reason for Recall

Potential for the Infusion Pump Administration Set to leak and/or disconnect at the bonded joint between the tubing and Injection Site (Y-Site).

Details

Recalling Firm
B. Braun Medical, Inc.
Units Affected
2580
Distribution
Distribution to US state of TX, and Canada.
Location
Allentown, PA

Frequently Asked Questions

What product was recalled?
B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032. Recalled by B. Braun Medical, Inc.. Units affected: 2580.
Why was this product recalled?
Potential for the Infusion Pump Administration Set to leak and/or disconnect at the bonded joint between the tubing and Injection Site (Y-Site).
Which agency issued this recall?
This recall was issued by the FDA Devices on October 2, 2019. Severity: Critical. Recall number: Z-2489-2019.