B. Braun Medical, Inc.: Medical Device Recall in 2015 - (Recall #: Z-0150-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Perifix Continous Epidural Anesthesia Pain Control Trays; Injection of anesthetics to provide regional anesthesia for pain management.

Product Classification:

Class II

Date Initiated: August 27, 2015

Date Posted: October 28, 2015

Recall Number: Z-0150-2016

Event ID: 72237

Reason for Recall:

Potential discoloration of the DuraPrep solution from unintended exposure to the sterilant during sterilization performed by the supplier.

Status: Terminated

Product Quantity: 433

Code Information:

Product Catalog Number: 332215 332262 530024 530132 551714 551879 555184 555259 Lot Number 0061417406 0061421878 0061416371 0061420212 0061413247 0061416388 0061416389 0061414413

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated