Philips North America Llc recalls Mammotrak Interventional Coil 1.5T
Recalled Product
Mammotrak Interventional Coil 1.5T
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: 453530228882; UDI-DI: 00884838066779; Serial No. 69, 82, 143, 64, 77, 87, 76, 81, 134, 124, 141, 103, 135, 138, 73, 72, 131.
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