Becton Dickinson & Company: Medical Device Recall in 2017 - (Recall #: Z-1897-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

BD FlowSmart Set MiniMed Pro-set Rx Only Distributed by Medtronic MiniMed Inc. 8006464633 8185765555 Legal Manufacturer Becton, Dickinson and Company USA BD Medical-Diabetes Care Becton Dickinson France SAS

Product Classification:

Class II

Date Initiated: December 23, 2016

Date Posted: May 10, 2017

Recall Number: Z-1897-2017

Event ID: 76294

Reason for Recall:

Patients are reporting high blood glucose (HBG) levels while using the MiniMed Pro-set and also noticed the catheter of the infusion set was bent/kinked.

Status: Terminated

Product Quantity: 57,750 units

Code Information:

6203871 30-Jun-19 6203860 30-Jun-19 6207535 30-Jun-19 6211649 31-Jul-19 6207537 30-Jun-19 6211650 31-Jul-19

Distribution Pattern:

US Distribution to the state of : CA

Voluntary or Mandated:

Voluntary: Firm initiated