Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled by B BRAUN MEDICAL INC Due to Potential for the lid of the catheter connector...
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 FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Open tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKF. Product Description: CE17TKF PERIFIX CONTIN. EPIDURAL TRAY
Quantity: 0 units
Why Was This Recalled?
Potential for the lid of the catheter connector to be in the incorrect position.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B BRAUN MEDICAL INC
B BRAUN MEDICAL INC has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report