Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Perifix¿ / Epidural anesthesia kit (10 count carton) Recalled by B. Braun Medical, Inc. Due to Kits were assembled with the incorrect Filter Straw.
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 kit (10 count carton)
Quantity: 16,070 units
Why Was This Recalled?
Kits were assembled with the incorrect Filter Straw.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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