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On August 6, the State Food and Drug Administration issued an announcement to notify Philips Kingway (Shenzhen) Industrial Co.
, Ltd.
of its voluntary recall of some of its products in violation of regulations
.
Including electrocardiograph
Details are as follows:
Philips Kingway (Shenzhen) Industrial Co.
, Ltd.
actively recalls ECG machines
, Ltd.
actively recalls ECG machines
Philips Kingway (Shenzhen) Industrial Co.
, Ltd.
reported that the lithium battery used with the product may overheat or burn after its service life
.
Philips Kingway (Shenzhen) Industrial Co.
The recall level is level two
.