Recalls — last 90 days
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips X7-2 transducer labelling for useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips X3-1 ultrasound transducer labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips S5-2 ultrasound transducer labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck your Philips S4-1 transducer labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips OMNI III TEE transducer expiration
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips OMNI II TEE transducer useful life label
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips ultrasound transducer useful life labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips L17-5 ultrasound transducer labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips L12-5 ultrasound transducer labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck your Philips C9-4 ultrasound transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Ultrasound, IncClass IIICheck Philips 3D6-2 transducer useful life labeling
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- 2026-04-01FDA-DevicePhilips Respironics, Inc.Class ICheck your Philips Respironics ventilator settings
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.
- 2026-04-01FDA-DevicePhilips Respironics, Inc.Class IStop using Philips Respironics Trilogy EV300 with non-pneumatic nebulizers
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.
- 2026-04-01FDA-DevicePhilips Respironics, Inc.Class ICheck your Philips Respironics ventilator settings
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.
- 2026-04-01FDA-DevicePhilips Respironics, Inc.Class ICheck your Philips Respironics Trilogy Evo ventilator
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.
- 2026-04-01FDA-DeviceOlympus Corporation of the AmericasClass IICheck your Olympus endoscope reprocessor compatibility
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
- 2026-04-01FDA-DeviceOlympus Corporation of the AmericasClass IICheck your Olympus endoscope reprocessor compatibility
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
- 2026-04-01FDA-DeviceOlympus Corporation of the AmericasClass IIStop using Olympus MAJ-1444 valve with OER reprocessors
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
- 2026-04-01FDA-DeviceOlympus Corporation of the AmericasClass IIStop using Olympus MAJ-1443 suction valve with OER reprocessors
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
- 2026-04-01FDA-DeviceBeckman Coulter, Inc.Class IIStop using Beckman Coulter MicroScan Neg MIC 56
Due to the likely presence of contamination in well(s).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck MRI safety if you have I.T.S. pelvic implant
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck if your implant needs MRI precautions
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck your surgical implant lot number
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck MRI compatibility of I.T.S. locking plates
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck MRI safety for I.T.S. ulna bone implants
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IIContact your surgeon about I.T.S. orthopedic plates
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck MRI safety if you have I.T.S. humeral plate
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck MRI safety if you have I.T.S. fibula plate
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck I.T.S. GmbH pelvic implants before MRI
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
- 2026-04-01FDA-DeviceI.T.S. GmbHClass IICheck I.T.S. surgical screws for MRI safety
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).