More than 50,000 devices are being recalled due to pinhole leaks associated with multiple risks. Customers should return any unused cannulae to Medtronic.

Cardiologists and vascular surgeons were previously told they could still use the device if necessary. Now, however, the message is that they should return the product to the manufacturer.

More than 750,000 devices are included in the new Class II recall. At this time, however, no devices need to be returned to the manufacturer. 

The Class II recall includes nearly 935,000 bottles of a medication that has been on the market for years. 

Healthcare providers should return any unused devices to the manufacturer. 

The same device was previously recalled back in 2022. Customers are urged to return any unused delivery systems included in the recall to Medtronic.

Trace amounts of blood were identified within the sealed packaging of these devices. No patients were exposed to the foreign material, and no adverse events were reported, but Medtronic is recalling the devices as a precaution.

Thousands of procedure kits used by cardiologists and cardiac surgeons are impacted by the new Class II recall. 

Patients given the drug in question could face an increased risk of blood vessel blockages or inflammation.