FDAClass IIDecember 20, 2017

Remisol Advance Software recall: Software Issue

Remisol Advance Software (Driver Architect) Catalog Number B32129 The Remisol Advance Data Manager (Stand alone Data Management Systems) collects and…

Why was Remisol Advance Software recalled?

Beckman Coulter has identified that due to a software nonconformity in connection with a changed service setting Remisol could display wrong results.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Version 1.6-1.9

Product
Remisol Advance Software (Driver Architect) Catalog Number B32129 The Remisol Advance Data Manager (Stand alone Data Management Systems) collects and…
Recalling firm
Normand Informatique
Quantity
34 units
Distribution
Worldwide Distribution - US Distribution and to the countries of : Australia, France, Germany, Israel and Russia
Recall date
December 20, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls