Medtronic Minimally Invasive Therapies Group: Medical Device Recall in 2018 - (Recall #: Z-1007-2018)

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:

MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays. Product Number: 8888222316.

Product Classification:

Class II

Date Initiated: October 14, 2017

Date Posted: March 21, 2018

Recall Number: Z-1007-2018

Event ID: 79319

Reason for Recall:

Medtronic is voluntarily recalling one lot of its MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays, Lot 1717900160, following notification from our supplier that one production lot of MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays was inadvertently shipped to Medtronic and distributed without being sterilized.

Status: Terminated

Product Quantity:

Code Information:

UDI: 10884521126473/20884521126470 Lot: 1717900160.

Distribution Pattern:

U.S.

Voluntary or Mandated:

Voluntary: Firm initiated