BD (Becton, Dickinson and Company) (NYSE:BDX) has voluntarily executed a product recall of certain lots ofBD Q-Syte™ Luer Access Devices and BD Nexiva™ Closed IV Catheter Systems. Use of the affected devices may cause an air embolism or leakage of blood and/or therapy, which may result in serious injury or death.
Creating memories for families by sharing information relating to children and parents with regard to activities, products, school, home and more.
BD Announces Worldwide Voluntary Recall ofBD Q-Syte™ Luer Access Devices and BD Nexiva™ Closed IV Catheter Systems
- Login or register to post comments
- Feed: Food and Drug Administration--Recalls
- Original article