B. Braun Medical, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1149-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, PERIFIX FX 19 Ga. Springwound Closed Tip Catheter, 5 mL Glass Luer Lock LOR Tray (Kit)-A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. Product Code: 332079

Product Classification:

Class II

Date Initiated: January 22, 2024

Date Posted: February 28, 2024

Recall Number: Z-1149-2024

Event ID: 93889

Reason for Recall:

Kits should contain Filter Straws with Standard Luer Connections however the kits contain Filter Straws with Neuraxial connectors preventing interface with the other components of the kit.

Status: Ongoing

Product Quantity: 3,480 units

Code Information:

UDI: 04046964177224 Lot Number: 0061855319 Exp. Date: 30.APR.2024

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated