Class I — Serious Health Hazard

Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

B.Braun Infusomat Space Volumetric Infusion Pump Administration Set Recalled by B. Braun Medical, Inc. Due to Potential for the Infusion Pump Administration Set to...

Date: May 1, 2019
Company: B. Braun Medical, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact B. Braun Medical, Inc. directly.

Affected Products

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

Quantity: 2580

Why Was This 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).

Where Was This Sold?

This product was distributed to 1 state: TX

Affected (1 state)Not affected

About B. Braun Medical, Inc.

B. Braun Medical, Inc. has 216 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report