FDAJanuary 13, 2020device

DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic Diagnostic Imaging System is applicable for adults, pregnant women, pediatric patients and neonates. It is intended for use in fetal, abdominal, pediatric, small organ (breast, thyro...

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

The hazard

The DP-30 displays an incorrect needle-guide bracket when used with the 65EC10EA model transducer.

What to do

FDA enforcement status: Terminated

Brands named

mindray ds usa inc dba mindray north americamindraymindray ds

Recall history

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

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DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic Diagnostic Imaging System is applicable for adults, pregnant women, pediatric patients and neonates. It is intended for use in fetal, abdominal, pediatric, small organ (breast, thyro... — Recall Details · AllClear