Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Tytek Medical Recalls TM-317 PneumoDart-Pneumothorax Needle Due to Fully and Partially Blocked Needles.pic.twitter.com/BhWemUNA2e

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Tytek Medical Recalls TM-317 PneumoDart-Pneumothorax Needle Due to Fully and Partially Blocked Needles. pic.twitter.com/BhWemUNA2e

Source: Food and Drug Adminstration (FDA): CDRHNew - February 25, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news