Recall database

Pump, Infusion, Implanted, Programmable recalls

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

Showing 1–2 of 2 recalls

Class IICompletedZ-2580-2026

Boston Scientific Corporation recalls Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump

There is the potential for leakage along the drug pathway from the pump through the end of the catheter.

Programmable Implanted Infusion Pump
Process control

Boston Scientific Corp…MNJul 1, 2026

Class IIOngoingZ-2201-2026

Medtronic Neuromodulation recalls Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest.…

Programmable Implanted Infusion Pump
Under Investigation by firm

Medtronic Neuromodulat…MNMay 20, 2026