Recall company profile

Simpleware Product Group, SYNOPSYS NORTHERN EUROPE Recalls

Overview of recall records associated with Simpleware Product Group, SYNOPSYS NORTHERN EUROPE, including dates, categories and classifications where available.

2recall records
Aug 18, 2021latest record date
Aug 18, 2021earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceAug 18, 2021

Simpleware ScanIP software recall — FDA Z-2253-2021

A issue (bug) has been identified with the interface and image software which could result in anatomical orientation tags/labels being displayed incorrectly. This could result in operator…

Class IIFDA: TerminatedSimpleware Product Group, SYNOPSYS NORTHERN EUROPE
Medical DeviceAug 18, 2021

Simpleware ScanIP medical software recall — FDA Z-2254-2021

A issue (bug) has been identified with the interface and image software which could result in anatomical orientation tags/labels being displayed incorrectly. This could result in operator…

Class IIFDA: TerminatedSimpleware Product Group, SYNOPSYS NORTHERN EUROPE

Understanding this recall history

This page summarizes recall records in which the official source identifies Simpleware Product Group, SYNOPSYS NORTHERN EUROPE as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.