This marks the latest recall-related issue for HeartMate in recent years. Last June, the FDA deemed another recall as serious ...

The Food and Drug Administration has identified a Class I recall of Q’Apel Medical 072 Aspiration System after the company ...

The Food and Drug Administration published a notice from Amneal Pharmaceutical that said the company is recalling two lots of ...

Medical device maker ICU Medical changed the designs of infusion pumps made in Minnesota without properly clearing important ...

The recall notice noted that the products all have the establishment number "Est. 46049" on the USDA mark of inspection. As of the day the recall was issued no injuries had been reported ...

On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or “the company”) voluntary recall of 1,617 units of its 072 Aspiration ...

Q’Apel Medical announced that the FDA classified a voluntary recall of its 072 A System as Class I, the most serious kind.

I’m not a paid consultant for them. You could say I’m an adviser,” said Chris Moore, who helped oust an Oakland mayor and an ...

according to a notice on the FDA’s website. The recall, which covers a 500-mg/100-ml dose of the drug packaged in infusion bags, is specifically concerned with particulate contamination by the ...