Texas recalls
1577 federal recalls on file affecting Texas - 165 Texas-specific plus 1412 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-01FDA-DevicePhilipsClass IIINationwideCheck 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-DevicePhilipsClass IIINationwideCheck 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-DevicePhilipsClass IIINationwideCheck 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-DevicePhilipsClass IIINationwideCheck 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-DevicePhilipsClass IIINationwideCheck 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-DevicePhilipsClass INationwideCheck 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-DevicePhilipsClass INationwideStop 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-DevicePhilipsClass INationwideCheck 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-DevicePhilipsClass INationwideCheck 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-DeviceOlympusClass IINationwideCheck 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-DeviceOlympusClass IINationwideCheck 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-DeviceOlympusClass IINationwideStop 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-DeviceOlympusClass IINationwideStop 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 CoulterClass IINationwideStop using Beckman Coulter MicroScan Neg MIC 56
Due to the likely presence of contamination in well(s).
- 2026-04-01FDA-DeviceI.T.SClass IINationwideCheck 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.SClass IINationwideCheck 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.SClass IINationwideCheck 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.SClass IINationwideCheck 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.SClass IINationwideCheck 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.SClass IINationwideContact 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.SClass IINationwideCheck 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.SClass IINationwideCheck 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.SClass IINationwideCheck 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.SClass IINationwideCheck 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).
- 2026-04-01FDA-DeviceI.T.SClass IINationwideCheck MRI compatibility of I.T.S. surgical 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.SClass IINationwideStop using I.T.S. GmbH olecranon plates 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.SClass IINationwideContact your doctor about I.T.S. GmbH Pilonplate
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.SClass IINationwideContact your surgeon about I.T.S. calcaneus 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.SClass IINationwideCheck MRI safety if you have this shoulder 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.SClass IINationwideContact your surgeon about I.T.S. clavicle plate
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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