JIANGSU JUMAO X-CARE Medical Equipment Co. issued a recall for the JMC5A Ni/Tru-Aire-5 Oxygen Concentrator after incidents of spontaneous fires. These fires could cause burns or worse. Patients are ...
In 2016, medical device giant Abbott issued a recall for its MitraClip cardiac device — "a Class I recall, the most serious type," the FDA said. "Use of this device may cause serious ...
The FDA today issued a notice informing customers of updated instructions for the Johnson & Johnson Abiomed Impella RP heart ...
sent all affected customers an urgent medical device correction and information about which patients may need their data reprocessed. This is a Class I recall, the FDA's most serious ...
The US Food and Drug Administration (FDA) has tagged a recall of breathing circuits manufactured by Sentec/Percussionaire as ...
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Over the past few years, companies in consumer goods industries have seen a concerning trend that presents a complex challenge: product recalls ... and medical devices. This absence of easily ...