Philips North America Llc recalls ST SENSE Breast Dx Coil
Recalled Product
ST SENSE Breast Dx Coil
Hazard / Issue
Potential safety issue where a patient may be harmed while preparing for or during a scan.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: REF: 453530264791; UDI-DI: 00884838066823; Serial No. 55, 3, 9, 36, 40, 56, 35, 39, 80, 46, 29, 7, 28, 55, 47, 54.
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