FDA recall Z-1471-2026

Abiomed, Inc. · Class I · device

Product

Impella RP. Product Code: 0046-0011.

Reason for recall

Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.

Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Canada, Croatia, Czechia, France, Germany, Hong Kong, Italy, Poland, Serbia, Switzerland.

Key facts

Status
Ongoing
Initiation date
2026-01-27
Report date
2026-03-11
Voluntary/Mandated
Voluntary: Firm initiated
Location
Danvers, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1471-2026