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