Health product recall

Automated Impella® Controllers (AIC)

Brand(s)
Last updated

Summary

Product
Automated Impella® Controllers (AIC)
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.  

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Automated Impella® Controllers (AIC)

IC13503

0042-0040-CA

Automated Impella® Controllers (AIC)

IC13266

0042-0040-CA

Automated Impella® Controllers (AIC)

IC11171

0042-0040-CA

Automated Impella® Controllers (AIC)

IC11172

0042-0040-CA

Automated Impella® Controllers (AIC)

IC1769

0042-0000-CA

Automated Impella® Controllers (AIC)

IC5821

0042-0000-CA

Automated Impella® Controllers (AIC)

IC5824

0042-0000-CA

Automated Impella® Controllers (AIC)

IC9416

0042-0000-CA

Automated Impella® Controllers (AIC)

IC9414

0042-0000-CA

Automated Impella® Controllers (AIC)

IC1179

0042-0000-US

Issue

Abiomed has decided to initiate a voluntary medical device recall (removal) for design changes that were previously implemented through the Abiomed field service process. Abiomed performed a retrospective review of Field Change Notices (FCN) and determined that certain AIC consoles in the field did not receive the updates introduced by FCN 113.
Failure to implement the applicable FCN 113 updates may result in the screen freezing during the Purge Cassette Change Wizard and the display of a false controller error.
These defects could delay the initiation of support during device set-up and, in high-risk patient populations, may lead to temporary inadequate hemodynamic support or a temporary loss of hemodynamic support. Hospital inventory may continue to be used to ensure continuity of care. Not all units are affected by this issue.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Abiomed Inc.

22 Cherry Hill Drive, Danvers, Massachusetts, United States, 01923

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-82721

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