WebNephron Pharmaceuticals, a generic drug maker, cited sterility issues as the cause of a voluntary nationwide recall of 2.1 million doses of medicine. WebURGENT MEDICAL DEVICE RECALL BD POSIFLUSH™ HEPARIN LOCK FLUSH SYRINGES BD™ PRE-FILLED NORMAL SALINE SYRINGES . April 20, 2024 . Product Name Catalog (REF) Number ... Saline Syringe (01)50382903065009 306500 708111D 735212A 120 units per case (30 units per shelf box)

RECALL ALERT: Mislabeled Insulin Syringes for Pets

WebSyringes and needles FDA notice for pen needles BD Flush Product Supply Disruption Enteral and anesthesia ISO changes Product Recalls Infusion Recall notification for Alaris System Infusion Pumps Software Recall notification for Alaris System Infusion Pumps BD Alaris System Hardware Recall Notification WebNational Center for Biotechnology Information horned hoodie baby blue

Class 2 Device Recall BD

Webfor certain Medfusion® 3500 and 4000 Syringe Pumps installed with the firmware versions listed in the affected device table above. Please note that this is a recall and not a product removal. As of May 13, 2024, a total of 53485 (world-wide) devices are included in this recall notification. This recall is being performed with the WebBD – Recall of BD Insulin Syringes with the BD Micro-Fine™IV Needle February 1, 2024 - BD announced a consumer-level recall of some lots of BD Insulin Syringes with the BD Micro … WebBD – Recall of BD Insulin Syringes with the BD Micro-Fine™IV Needle February 1, 2024 - BD announced a consumer-level recall of some lots of BD Insulin Syringes with the BD Micro-Fine IV Needle because of manufacturing issues that can result in unsealed packaging for the individual syringes. horned hoodies