FDAClass IIAugust 11, 2021

Sharesource Connectivity Platform for Use with the Amia recall

Sharesource Connectivity Platform for Use with the Amia Automated PD System

Why was Sharesource Connectivity Platform for Use with the Amia recalled?

Baxter Healthcare Corporation has identified that the AMIA Sharesource User Guide that is used with the AMIA Automated PD System cyclers incorrectly describes the function of the UF (Ultrafiltration) Limit setting as the ending criteria of the cyclers Extra Last Drain Mode. In some locations in the guide, it states that the UF volume achieved must exceed the programmed UF Limit before the cycler will end the Extra Last Drain, allowing the patient to end therapy or proceed to their last fill.

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?

Product Code 5C9400, UDI: 45413765565692, 55413765565699

Product
Sharesource Connectivity Platform for Use with the Amia Automated PD System
Recalling firm
BAXTER HEALTHCARE CORPORATION
Quantity
1 unit
Distribution
Worldwide distribution - US Nationwide distribution and the country of Japan.
Recall date
August 11, 2021
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls