Loading...
Loading...
All product recalls associated with Sonosite, Inc..
Total Recalls
6
Past Year
0
Class I (Serious)
0
Most Recent
Aug 2008
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The TEE transesophageal transducer, when connected to a SonoSite M-Turbo Ultrasound System, may exhibit erratic operation of the Scanplane Orientation Indicator on the system display. The indicator may move erratically and not accurately represent the orientation of the TEE transducer array.
Sterilization of the SonoSite LAP surgical Transducer with the Sterrad NX System may result in damage to the transducer.
Sterilization of the SonoSite SLT ultrasound surgical transducer with the Sterrad NX System may result in damage to the transducer.
Laparoscopic transducer exceeds the limits specified for radio-frequency emissions by up to 10db.
22 gauge needle guides were intermixed with 21 gauge guides and labeled as 21 gauge needle guides.
When SonoCalc IMT 3.0 software is used with the SonoSite 180Plus ultrasound system, the software miscalculates the intima-media-thickness, a measurement of risk for cardiovascular or cerebrovascular events. Underestimates percentage of stenosis, false negative result.