Embolic Device Recall Issued by Medtronic After Deaths Linked to Pipeline Vantage Models
Fremont, California – The FDA has issued a serious recall for certain Medtronic Pipeline Vantage embolization devices following multiple deaths linked to the product. The affected devices, known as the Pipeline Vantage 027 models, are being removed from use and sale, with updated instructions also being implemented for the Pipeline Vantage 021 models. These devices, … Read more