Covidien LLC: Medical Device Recall in 2015 - (Recall #: Z-2545-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item Code:22550PC

Product Classification:

Class II

Date Initiated: August 19, 2015

Date Posted: September 9, 2015

Recall Number: Z-2545-2015

Event ID: 71963

Reason for Recall:

Multi-Function Defibrillation Electrodes, Pre connect- potential for damage to the wire insulation may result in a potentially increased risk for reduced or no patient therapy and patient and/or clinician burns

Status: Terminated

Product Quantity: 7660 sets

Code Information:

Lot Numbers: 517521X, 519835X

Distribution Pattern:

Nationwide Foreign: Canada Australia Denmark Germany New Zealand

Voluntary or Mandated:

Voluntary: Firm initiated