Zyno Medical Infusion Pump Recall Due to Deadly Risk of Air Embolism
Manufacturer is instructing medical providers to stop using certain Zyno infusion pumps until a new software update is installed, following reports of injury.
Manufacturer is instructing medical providers to stop using certain Zyno infusion pumps until a new software update is installed, following reports of injury.
FDA has categorized the action as a Class I Medical Device Recall, after dozens of reports involving problems with Abbott cardiac catheters leaking air inside a patient’s bloodstream, resulting in a risk of serious injury or death