B. Braun Medical, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1021-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Design Options COMBINED SPINAL/EPIDURAL TRAY- Intended for administration of analgesic/anesthetic agent to intrathecal space and epidural space for pain control. Model/Catalog Number: 530159

Product Classification:

Class II

Date Initiated: December 4, 2024

Date Posted: February 5, 2025

Recall Number: Z-1021-2025

Event ID: 95874

Reason for Recall:

Incorrect catheter connector within the kit resulting in inability to provide a secure connection to the epidural catheter. The incorrect catheter connector is smaller than the required catheter connector and therefore is unable to be used to administer medication.

Status: Ongoing

Product Quantity: 1090 units

Code Information:

UDI-DI 04046964669286 (Primary); 04046964669279 (Unit of Use); Lot Number 0061916572

Distribution Pattern:

US Nationwide distribution in the states of MO, OK.

Voluntary or Mandated:

Voluntary: Firm initiated