Class IIIOngoingZ-1621-2026
Philips Ultrasound, Inc recalls Philips L17-5 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound, In…PAApr 1, 2026
All device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,057–1,068 of 4,586 recalls
Class IIIOngoingZ-1620-2026
Philips Ultrasound, Inc recalls Philips L12-5 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound, In…PAApr 1, 2026
Class IIIOngoingZ-1619-2026
Philips Ultrasound, Inc recalls Philips C9-4 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound, In…PAApr 1, 2026
Class IIIOngoingZ-1618-2026
Philips Ultrasound, Inc recalls Philips 3D6-2 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound, In…PAApr 1, 2026
Class IOngoingZ-1617-2026
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo Universal
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics, I…PAApr 1, 2026
Class IOngoingZ-1616-2026
Philips Respironics, Inc. recalls Philips Respironics Trilogy EV300
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics, I…PAApr 1, 2026
Class IOngoingZ-1615-2026
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo O2
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics, I…PAApr 1, 2026
Class IOngoingZ-1614-2026
Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics, I…PAApr 1, 2026
Class IIOngoingZ-1613-2026
Olympus Corporation Of The Americas recalls Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of…PAApr 1, 2026
Class IIOngoingZ-1612-2026
Olympus Corporation Of The Americas recalls Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of…PAApr 1, 2026
Class IIOngoingZ-1611-2026
Olympus Corporation Of The Americas recalls Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of…PAApr 1, 2026
Class IIOngoingZ-1610-2026
Olympus Corporation Of The Americas recalls Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of…PAApr 1, 2026