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The Food and Drug Administration announced that Philips recalled the software following 109 reported injuries and two ...
The FDA is elevating a recall from Philips related to one of its wearable outpatient heart monitors, used to help detect cases of hidden, transient arrhythmias that may only last minutes at a time.
Philips is recalling the software associated with its mobile cardiac outpatient telemetry devices after 109 patient injuries and two patient deaths, a Jan. 13 FDA recall notice said. The software ...
to immediately cease the sale of certain products manufactured by affiliates of Philips Lighting brand, and also ordered the recall and destruction of infringing products distributed in the market ...
The AAP chief assisted with filling out registration forms and handed over ‘Kejriwal Kavach Cards’ to the beneficiaries. The AAP said the card guarantees benefits under the Sanjeevani Yojana ...
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