ClearanceBrief
Recall Z-1842-2020 ยท ITX Transducer, Ultrasonic, Diagnostic

Philips Ultrasound Inc

Transducer S7-3t UDI (01)00884838067530 REF 989605439232 Used as accessory with: iE33, HD11 Ultrasound Systems - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography (TEE) studies

DateAug 30, 2019
StatusTerminated
ReasonThe firm has discovered an issue associated with some Transesophageal (TEE) transducers that were not properly programmed during manufacturing. As a result, the system is unable to correctly measure the temperature on the distal tip of the transducer. This issue may result in affected transducers not initiating auto-cool during use which could result in patient injury
Root causeProcess control
ActionIf you have an EPIQ, Affiniti or iE33 system, verify that all your S7-3t and S8-3t TEE transducers are programmed properly by connecting them to the system, checking the transducer temperature (TEE T) on the display, and following the instructions provided on this letter. If you determine that your transducer is not properly programmed, discontinue using the transducer immediately and contact your local Philips representative to schedule an appointment with a field service engineer. If you have an HD11 or CX50 system discontinue using the S7-3t and S8-3t transducer immediately and contact yo
DistributionWorldwide distribution - US Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K030455BORIS PLATFORM DIAGNOSTIC ULTRASOUND SYSTEM
Philips Ultrasound, Inc., Mar 13, 2003
K043535HD11 DIAGNOSTIC ULTRASOUND SYSTEM
Philips Ultrasound, Inc., Jan 6, 2005