B. Braun Medical, Inc.: Medical Device Recall in 2018 - (Recall #: Z-3362-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

CE18TK ACCU-BLOC PERIFIX KIT, Material Number 332220 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.

Product Classification:

Class II

Date Initiated: July 20, 2018

Date Posted: October 10, 2018

Recall Number: Z-3362-2018

Event ID: 80811

Reason for Recall:

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.

Status: Terminated

Product Quantity: 63980

Code Information:

Batch: 61595170, 61595613, 61596536, 61598356, 61597084, 61600180, 61617168, 61616702, 61617169, 61616703, 61614599, 61616701, 61616700, 61614596, 61614598, 61619583, 61620763, 61622163, 61621828

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated