B. Braun Medical, Inc. recalls EC19OF SPRINGWOUND 19G EPID CATHETER, Material Number 333514 Connection device used by physicians to provide various

Recalled October 10, 2018 · FDA recall Z-3398-2018 · B. Braun Medical

Hazard

The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed. · FDA Class II

Units

1000

Sold at

Worldwide Distribution: US (nationwide) and countries of: Australia, Canada, Guatemala and Kuwait.

Description

The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.

Product

EC19OF SPRINGWOUND 19G EPID CATHETER, Material Number 333514 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

Manufacturer(s)

B. Braun Medical, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →