Medtronic Vascular: Medical Device Recalls in 2014

According to to data from the FDA, there were 2 medical device recalls made by Medtronic Vascular in 2014. See the details of the recalls below.

You can see similar recalls for other firms.

• Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
• Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a manometer with measuring pressures ranging from vacuum to 20bars in 0.5 bar increments. The Everest 30atm Device is outfitted with a manometer with measuring pressures ranging from vacuum to 30bars in 0.5 bar increments. The manometers are accurate to within +/- 3% of the gauges full scale. The device is a sterile, single use device and is not implanted; it also does not come in direct contact with the patient. This product is packaged in an inner and outer Tyvek /poly layer pouch.