Philips Medical Systems, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1439-2014)

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:

Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.

Product Classification:

Class II

Date Initiated: March 31, 2014

Date Posted: April 16, 2014

Recall Number: Z-1439-2014

Event ID: 67857

Reason for Recall:

A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy

Status: Terminated

Product Quantity: 19 units

Code Information:

Serial Numbers: USN1307680 USD1309181 USD1308456 USD1309182 USD1309167 USD1309184 USD1309168 USD1309194 USD1309180 USD1309195 USD1309196 USD1309274 USD1309197 USD1309286 USD1309227 USD1309301 USD1309264 US11409686 USD1309269

Distribution Pattern:

Worldwide Distribution - US Distribution including the states of IN and WA., and the countries of : CHINA FRANCE GERMANY ITALY MALAYSIA PANAMA SAUDI ARABIA TURKEY and UNITED KINGDOM.

Voluntary or Mandated:

Voluntary: Firm initiated