Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Perifix Continous Epidural Anesthesia Pain Control Trays Recalled by B. Braun Medical, Inc. Due to Potential discoloration of the DuraPrep solution from unintended...

Date: August 27, 2015
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

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

Quantity: 433

Why Was This Recalled?

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

Where Was This Sold?

Nationally

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