Philips North America Llc recalls Mammotrak Diagnostic Coil 3.0T
Recalled Product
Mammotrak Diagnostic Coil 3.0T
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: 453530228911; UDI-DI: 00884838066786; Serial No. 91, 130, 80, 53, 90, 11, 58, 25, 51, 4, 67, 34.
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