FDA-Device2026-04-01Class IIIMISBRANDING
Philips L17-5 Ultrasound Transducer recalled for labeling clarification on useful life
EXPIRATION DATE ERRORNationwide distribution
Check Philips L17-5 ultrasound transducer labeling
Philips is clarifying labeling on certain L17-5 Ultrasound Transducers to better define their useful life in clinical use. This affects 2 units with specific model and serial numbers distributed nationwide. No injuries have been reported.
- If you operate a healthcare facility with the affected transducers (Models 989605366371 or 989605388061, Serial Nos. 03228X or 03360Q), contact Philips for labeling clarification
- Review updated labeling guidance from Philips regarding transducer useful life and maintenance
Hazard
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Sold states
US Nationwide distribution.
Affected count
2 units
Manufactured in
1 Echo Dr, Reedsville, PA, United States
Products
Philips L17-5 Ultrasound Transducer
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1621-2026More Philips Ultrasound, Inc recalls
- FDA-Device2026-04-01Philips S5-2 Ultrasound Transducer recalled for clarification on useful life labeling
- FDA-Device2026-04-01Philips S4-1 Ultrasound Transducer recalled for clarification of useful life labeling
- FDA-Device2026-04-01Philips X3-1 ultrasound transducer recalled for labeling clarification on device lifespan
- FDA-Device2026-04-01Philips OMNI II TEE Ultrasound Transducer recalled for useful life labeling clarification
- FDA-Device2026-04-01Philips Mini Multi TEE Ultrasound Transducer recalled for labeling clarification on useful life
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