Z-0122-2026 Class II Ongoing
FDA device recall Z-0122-2026 was initiated by B BRAUN MEDICAL INC on September 18, 2025 and is designated Class II. Reason for recall: Potential for the lid of the catheter connector to be in the incorrect position. The recall status is ongoing. Affected quantity: 10,130 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 15, 2025
- Initiation Date
- September 18, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10,130 units
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.
Reason for Recall
Potential for the lid of the catheter connector to be in the incorrect position.
Distribution Pattern
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.
Code Information
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.