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FDAAugust 12, 2026

Abiomed Automated Impella Controller Recall Over Purge Cassette Recognition Issues

FDA published this notice on August 12, 2026 for United States.

This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.

What AreaZine recorded

Agency
FDA
Place
United States
Date
August 12, 2026
Recall class
Class I
Reason given by the agency
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
Distribution
Domestic: Nationwide Distribution. International: United Arab Emirates, Austria, Australia, Belgium, Brunei Darussalam, Brazil, Canada, Switzerland, Chile, China, Colombia, Costa Rica, Cyprus, Czechia, Germany, Denmark, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Croatia, Hungary, Ireland, Israel, India, Italy, Japan, Kuwait, Luxembourg, Mexico, Malaysia, Netherlands, Norway, New Zealand, Panama, Pakistan, Poland, Serbia, Saudi Arabia, Sweden, Singapore, Slovenia, Thailand, Taiwan;
Official source
the notice at its source

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Source: FDA.

The record around this notice