Recall StatusOpen, Classified
Date Initiated2023-12-07
Product Quantity55 US; 1029 ROW
Reason for Recall
If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently as part of daily operation, the connector and wire may disconnect from the welding point, which may result in intermittent loss of the ECG signal. Loss of ECG signal may lead to the decision to rescan the patient or delay in diagnosis during a clinical emergency.
Firm Action
On December 7, 2023, the firm notified affected customers through URGENT Medical Device Correction Notice letters.
Customers were informed that they may continue to use their Philips Incisive CT system in accordance with the intended use. However, to minimize the potential for loss of the ECG signal, customers should avoid frequently plugging and unplugging the PIM cable. In case of a connection failure, contact your local service representative and reference FCO72800782.
Philips will contact you to schedule time for a Field Service Engineer to visit your site to replace the PIM cable with an upgraded version.
If you need additional information or support concerning this issue, please contact Philips' Customer Care Solutions Center at 1-800-722-9377.
Root Cause
Component design/selection
Distribution Pattern
Domestic distribution to the following states: AL
CA
CO
FL
GA
HI
IL
IN
KS
KY
LA
MD
MI
MO
MS
ND
NE
NJ
NY
OH
OK
PA
RI
SC
TX
UT
VT
WA
International distribution worldwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.