Maquet Cardiovascular, LLC: Medical Device Recalls in 2022

According to to data from the FDA, there were 3 medical device recalls made by Maquet Cardiovascular, LLC in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
• INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic graft, and cardioroot configurations designed for use on the thoracic aorta
• HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070