Recall
FDAHealthSeptember 18, 2025

B BRAUN MEDICAL INC — 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 Cathete

⚠️ Potential for the lid of the catheter connector to be in the incorrect position.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
September 18, 2025

Nationwide distribution to AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV.

What's affected?

Product
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
Lot code
0062011669

Additional details

REF: 332086; Product Code: CE17TKF; UDI-DI (Primary): 04046955900985; UDI-DI (Unit of Use): 04046955900992; Lot Number: 0062011669. Expiration Date: 07/31/2026.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 0 units.

View original FDA notice →

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