Today, the @US_FDA identified a Class I Recall, the most serious type of recall: LeMaitre Vascular Inc. Recalls LeMaitre Over the Wire Embolectomy Catheter Due to Balloon Deflation and Separation Issue.pic.twitter.com/5oGWz05q3P

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: LeMaitre Vascular Inc. Recalls LeMaitre Over the Wire Embolectomy Catheter Due to Balloon Deflation and Separation Issue. pic.twitter.com/5oGWz05q3P

Source: Food and Drug Adminstration (FDA): CDRHNew - April 2, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news