B. Braun Medical, Inc.: Medical Device Recall in 2013 - (Recall #: Z-2166-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Outlook Safety Infusion System Burette Set. For intravenous fluid administration.

Product Classification:

Class II

Date Initiated: August 5, 2013

Date Posted: September 18, 2013

Recall Number: Z-2166-2013

Event ID: 65993

Reason for Recall:

Reports were received of an incorrectly assembled Outlook Safety Infusion System Burette Set (Product Code 375038), and the investigation determined that one of the ULTRASITE injection sites and corresponding low pressure backcheck valve was assembled upside down.

Status: Terminated

Product Quantity: 900

Code Information:

Catelog Number 375038, Lot Number 0061317318, Expiration Date: 04/30/2016

Distribution Pattern:

Distributed in the states of FL, NY, NJ, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated