Jaundice Meters Subject to FDA Class I Recall Jaundice Meters Subject to FDA Class I Recall

Draeger Medical Systems, Inc, has recalled more than 4500 JM-103 and JM-105 jaundice meters because users have misinterpreted display messages, leading to serious injuries.News Alerts

Source: Medscape ObGyn and Womens Health Headlines - June 26, 2018 Category: OBGYN Tags: Pediatrics News Alert Source Type: news