Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1579-2015 — 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 (

U.S. FDA — Device Enforcement · United States · 2015-04-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1579-2015
Date of alert
2015-04-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Ultrasound, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
989605386721
Reported risk: 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).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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