Recall database

Recalls: Under Investigation by firm

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 301–312 of 1,121 recalls

Class IOngoingZ-1471-2026

Abiomed, Inc. recalls Impella RP. Product Code: 0046-0011.

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

Abiomed, Inc.MAMar 11, 2026

Class IOngoingZ-1470-2026

Abiomed, Inc. recalls Impella RP Flex with SmartAssist. Product Code: 1000323.

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

Abiomed, Inc.MAMar 11, 2026

Class IOngoingZ-1469-2026

Abiomed, Inc. recalls Impella RP with SmartAssist. Product Code: 0046-0035.

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

Abiomed, Inc.MAMar 11, 2026

Class IIOngoingZ-1474-2026

Remel, Inc recalls Campy CVA Medium 100/PK

Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

Remel, IncKSMar 4, 2026

Class IIOngoingZ-1473-2026

Medtronic Perfusion Systems recalls Octopus Nuvo Tissue Stabilizer

During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top…

Medtronic Perfusion Sy…MNMar 4, 2026

Class IIOngoingZ-1457-2026