FDAAugust 30, 2019device

Transducer S8-3t UDI (01)00884838067523 REF 989605420183 Can be used with: iE33 Utrasound System - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography (TEE) studies

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The 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

What to do

FDA enforcement status: Terminated

Brands named

philips ultrasoundphilips

UPCs

00884838067523989605420183

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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