RecallRadar

FDA Device recall Z-1579-2015

EPIQ 7 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 7G, EPIC 7C, EPIQ 7W. Catalog Number: 795200 / 795201

On 2015-05-13 the FDA classified a Class II recall of EPIQ 7 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 7G, EPIC 7C, EPIQ 7W. Catalog Number: 795200 / 795201 by Philips Ultrasound, citing when Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set up to Metric and weight and/or height is entered, a unit conversion error may result in the incorrect c….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1579-2015
ClassificationClass II
Statusterminated
Initiated2015-04-10
Published2015-05-13
Last updated2026-09-13 11:53 UTC
CompanyPhilips Ultrasound
DistributionUS

Product

EPIQ 7 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 7G, EPIC 7C, EPIQ 7W. Catalog Number: 795200 / 795201. Part Number: 989605386721 With: 453561726491 (1.0) 453561728121 (1.0.1) 453561736781 (1.1) 453561750021 (1.1.1) 453561753631 (1.1.2) 453561772251 (1.2) 453561772631 (1.2.1) 453561786591 (1.2.2) 453561785101 (1.3) 453561800601 (1.3.1) 453561805211 (1.3.2)

Reason

When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set up to Metric and weight and/or height is entered, a unit conversion error may result in the incorrect calculation of the patients Body Surface Area (BSA).

Identifiers

code_info
************************SYSTEM CODES IN THE US**************************** US114B0149, US114B0158, US114B0159, US114…************************SYSTEM CODES IN THE US**************************** US114B0149, US114B0158, US114B0159, US114B0161, US114B0168, US114B0169, US114B0171, US114B0172, US114B0186, US114B0223, US114B0225, US114B0226, US114B0227, US114B0228, US114B0229, US114B0268, US114B0269, US114B0304, US114B0305, US114B0306, US114B0307, US114B0336, US114B0337, US114B0356, US114B0357, US114B0358, US114B0359, US114B0360, US114B0395, US114B0399, US114B0402, US114B0434, US114B0436, US114B0437, US114B0440, US114B0441, US114B0462, US114B0463, US114B0464, US114B0465, US114B0466, US114B0467, US114B0472, US114B0477, US114B0478, US114B0490, US114B0491, US114B0492, US114B0510, US114B0511, US114B0530, US114B0543, US114B0571, US114B0572, US114B0579, US114B0580, US114B0581, US114B0581, US114B0581, US114B0582, US114B0582, US114B0596, US114B0597, US114B0599, US114B0600, US114B0601, US114B0602, US114B0603, US114B0604, US114B0616, US114B0617, US114B0618, US114B0623, US114B0650, US114B0651, US114B0668, US114B0669

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1579-2015%22

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