← Back to recalls
FDA DeviceClass INotable

FDA Recall: Impella RP. Product Code: 0046-0011.

Date: 2026-03-11
Brand: Abiomed, Inc.
Category: Medical Device
FDA Class: Class I

Description

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

Hazard

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

Remedy

179 units

View original recall →
FDA Recall: Impella RP. Product Code: 0046-0011. | RecallWatch