FDA recall Z-2375-2025
Philips Ultrasound, Inc · Class III · device
Product
L12-5 38mm Transducer Probe
Reason for recall
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Distribution
US Nationwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2025-07-03
- Report date
- 2025-09-03
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Reedsville, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2375-2025