← FDA ENFORCEMENT
Z-0122-2026Class II

B BRAUN MEDICAL INC

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
B BRAUN MEDICAL INC
Product type
Device
Status
Ongoing
Report date
2025-10-15
Distribution
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.
Firm state
PA
Product quantity
10,130 units
Initiated by
Voluntary: Firm initiated
Reason for recall

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

Product description

ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 25 Ga. x 5 in. (12.7 cm) Spinal Needle with Marking and Centering Sleeve, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: ES1725KFX. Product Description: ES1725KFX ESPOCAN SPINAL/EPID. TRAY.

Code / lot info

REF: 333196; Product Code: ES1725KFX; UDI-DI (Primary): 04046955899531; UDI-DI (Unit of Use): 04046955899548; Lot Numbers: 0062005817, 0062011662, 0062011663, 0062014354, 0062011664. Expiration Date: 07/31/2026.

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →