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Philips Ultrasound, Inc recalls Philips Mini Multi TEE Ultrasound Transducer
Recalled April 1, 2026 · FDA recall Z-1622-2026 · Philips Ultrasound
Hazard
To provide clarification and labelling to define the useful life of ultrasound transducers in the field. · FDA Class III
Units
11 units
Sold at
US Nationwide distribution.
Description
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Product
Philips Mini Multi TEE Ultrasound Transducer
Manufacturer(s)
Philips Ultrasound, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →