Skip to content
Recall Observatory FDA recall evidence

Device 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.

Z-3398-2018

July 20, 2018

Class II

Product summary

Firm
B. Braun Medical, Inc.
Event
Event 80811
Status
Terminated
Classification
Class II
Quantity
1000
Official record key
device-enforcement:Z-3398-2018

Official wording

Reason: 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.

Code information: Batch: 61609096, 61616890

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.