Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Perifix¿ / Epidural anesthesia set Recalled by B. Braun Medical, Inc. Due to Mislabeling
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¿ / Epidural anesthesia set, medicated
Quantity: 3440 units
Why Was This Recalled?
Product may be mislabeled with an incorrect lid stock label.
Where Was This Sold?
This product was distributed to 13 states: AZ, AR, CA, FL, GA, IL, MA, MO, NJ, NC, PA, TX, WA
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