B. Braun Medical, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1150-2024)

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, 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. It includes the pharmaceutical anesthetic agent and a needle, with additional devices utilized for the procedure (e.g., syringe, dressings), and may include a catheter (i.e., may be intended for single- or continuous-administration). It is not intended for intrathecal anesthesia. Product Code: 332248

Product Classification:

Class II

Date Initiated: January 22, 2024

Date Posted: February 28, 2024

Recall Number: Z-1150-2024

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: 3,890 units

Code Information:

UDI: 04046964178689 Lot Number: 0061855122 Exp. Date: 25.OCT.2024

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated