The U.S. Food and Drug Administration is recalling 89,312 bottles of NasoGel nasal spray because the product might cause ...

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 ...

The FDA today issued a notice informing customers of updated instructions for the Johnson & Johnson Abiomed Impella RP heart pump.

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 injuries or ...

The US Food and Drug Administration (FDA) has tagged a recall of breathing circuits manufactured by Sentec/Percussionaire as ...

Medical device recalls, whether voluntary or mandated, are crucial for ensuring patient safety. Here are three recent recalls reported to the FDA: Phillips recalls monitoring service application ...

The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.

The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...

Product recalls are a major headache for pharma ... with extensive experience in medical device, biotechnology and pharmaceutical marketing. A graduate of the University of Texas, Amy joined ...

While the increase in recalls alone would be enough cause ... including pharmaceuticals and medical devices. This absence of easily accessible, credible safety information creates a significant ...

Med-tech firms have gnashed their teeth for decades over the use of the term “recall,” given that some recalls are mere corrections to product labels while others entail a full product withdrawal. The ...