Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun Medical, Inc. Due to Kits should contain Filter Straws with Standard Luer...
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
Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX FX 19 Ga. Springwound Closed Tip Catheter, 5 mL Glass Luer Lock LOR Tray (Kit)-A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. Product Code: 332079
Quantity: 3,480 units
Why Was This Recalled?
Kits should contain Filter Straws with Standard Luer Connections however the kits contain Filter Straws with Neuraxial connectors preventing interface with the other components of the kit.
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