Recall StatusTerminated
Date Initiated2014-02-18
Date Terminated2020-09-11
Product Quantity3541 units
Reason for Recall
MRx may display a Red X in the Ready For Use (RFU) indicator during automated tests informing the user that a failure has been detected that may prevent the delivery of a shock and pacing
Firm Action
Philips Healthcare issued and Urgent Medical Device Correction notification/Field Safety Notice on 02/18/14 to inform customers of the issue,
Philips is asking customers to follow the Action to be Taken by Customer/User section of the Urgent Medical Device Correction notification/Field Safety Notice:
You can continue to use your MRx prior to receiving the hardware upgrade, provided that if you observe that the MRx is displaying a Red X in the Ready For Use (RFU) indicator\during automated tests, a failure has been detected that may prevent the delivery of a shock or pacing due to this issue.
If this is observed you should turn the Therapy Knob to Monitor. An INOP message describing the failure is displayed. If needed, run an Operational Check for further information. If the condition persists, take the device out of use and call for service.
Identify a readily available backup defibrillator to use in the event the affected HeartStart MRx fails to deliver therapy.
Philips will perform a hardware upgrade (replace therapy boards) free of charge to be installed by a Philips Field Service Engineer. Contact your local Philips representative or call us at 1-800-722-9377.
Root Cause
Component design/selection
Distribution Pattern
Nationwide
Foreign:
AUSTRIA
BAHRAIN
BELGIUM
BRAZIL
CANADA
CHINA
EGYPT
ESTONIA
FINLAND
FRANCE
GERMANY
GHANA
ICELAND
INDIA
INDONESIA
IRELAND
ISRAEL
ITALY
JAPAN
JORDAN
KENYA
KOREA, REPUBLIC OF
LATVIA
LEBANON
LIBYAN ARAB JAMAHIRIYA
LITHUANIA
MALAYSIA
MEXICO
MOZAMBIQUE
MYANMAR (Burma)
NETHERLANDS
NETHERLANDS ANTILLES
NEW CALEDONIA
NEW ZEALAND
NORWAY
PAKISTAN
PERU
POLAND
PORTUGAL
QATAR
RUSSIAN FEDERATION
SAUDI ARABIA
SINGAPORE
SOUTH AFRICA
SPAIN
SWEDEN
SWITZERLAND
TAIWAN, PROVINCE OF CHINA
THAILAND
TURKMENISTAN
UNITED ARAB EMIRATES
UNITED KINGDOM
VIET NAM
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.