Medtronic Vascular: Medical Device Recall in 2014 - (Recall #: Z-0205-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K

Product Classification:

Class II

Date Initiated: October 13, 2014

Date Posted: November 19, 2014

Recall Number: Z-0205-2015

Event ID: 69488

Reason for Recall:

Two reports have been received on the 6F launcher Guide Catheter lot (Model Number LA6JR40K; lot No 0007244836} for incorrect usable length of the Guide Catheter. It was reported that the catheters had a usable length of 90 cm instead of 55 cm, which was specified on the packaging label. Usable length is defined as the total length of catheter shaft from the distal end of the strain relief to the

Status: Terminated

Product Quantity: 11 devices

Code Information:

Lot Number: 0007244836 MODEL: LA6JR40K

Distribution Pattern:

US Distribution including the states of NC, IA, IL and KS.

Voluntary or Mandated:

Voluntary: Firm initiated