-
GE Healthcare CARESTATION 750 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 750 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650c A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650C A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650C A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 650 SE, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 650 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 620 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare Carestation 620 SE, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 620 A2, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
GE Healthcare CARESTATION 620 A1, Model recall
FDA
· GE Medical Systems China Co., Ltd. · Class I
-
Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model recall
FDA
· Conavi Medical Inc. · Class I
-
HeartMate Mobile Power Unit recall
FDA
· Thoratec LLC · Class I
-
AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform… recall
FDA
· ZOLL Circulation, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Tandem Mobi Insulin Pump with Interoperable Technology recall
FDA
· Tandem Diabetes Care, Inc. · Class I
-
t:slim X2 Insulin Pump with Interoperable Technology recall
FDA
· Tandem Diabetes Care, Inc. · Class I
-
BD 4 Fr Single-Lumen PowerPICC Catheters recall
FDA
· Bard Access Systems, Inc. · Class I
-
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration… recall
FDA
· Qapel Medical Inc. · Class I
-
Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY recall
FDA
· Medline Industries, LP · Class I
-
Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
FDA
· Medline Industries, LP · Class I
-
Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
FDA
· Medline Industries, LP · Class I
-
Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
FDA
· Medline Industries, LP · Class I
-
Medline medical procedure kits, containing Medtronic Aortic Root Cannula… recall
FDA
· Medline Industries, LP · Class I
-
Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model recall
FDA
· Draeger, Inc. · Class I
-
Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model recall
FDA
· Draeger, Inc. · Class I
-
Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model recall
FDA
· Draeger, Inc. · Class I
-
Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model recall
FDA
· Draeger, Inc. · Class I
-
Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model recall
FDA
· Draeger, Inc. · Class I
-
ID Circuit Product Name: ID Circuit Flex 220 Model recall
FDA
· Draeger, Inc. · Class I
-
VentStar Product Name: VentStar Flex 220 Model recall
FDA
· Draeger, Inc. · Class I
-
CVAC Aspiration System recall
FDA
· Calyxo, Inc. · Class I
-
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable… recall
FDA
· Covidien, LP · Class I
-
smiths medical ProPort Low Profile Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Low Profile Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System, PolyFlow Catheter… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System, Silicone Catheter… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
smiths medical ProPort Plastic Venous Access System, Silicone Catheter… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
Aortic Root Cannula: 1. DLP Aortic Root Cannula A… recall
FDA
· Medtronic Perfusion Systems · Class I
-
BD Care Coordination Engine (CCE) Infusion Adapter… recall
FDA
· CareFusion 303, Inc. · Class I
-
BD Alaris Systems Manager recall
FDA
· CareFusion 303, Inc. · Class I
-
Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035… recall
FDA
· Smiths Medical ASD, Inc. · Class I
-
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software… recall
FDA
· Baxter Healthcare Corporation · Class I
-
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX recall
FDA
· Baxter Healthcare Corporation · Class I