Philips North America Llc recalls Mammotrak Interventional Coil 3.0T
Recalled Product
Mammotrak Interventional 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: 453530228891; UDI-DI: 00884838065857; Serial No. 73, 96, 58, 95, 119, 26, 16, 56, 94, 38, 28, 66, 135, 120, 2, 76.
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