-
BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 recall
FDA
· Olympus Corporation of the Americas · Class I
-
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 recall
FDA
· Olympus Corporation of the Americas · Class I
-
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 recall
FDA
· Olympus Corporation of the Americas · Class I
-
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 recall
FDA
· Olympus Corporation of the Americas · Class I
-
EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 recall
FDA
· Olympus Corporation of the Americas · Class I
-
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 recall
FDA
· Olympus Corporation of the Americas · Class I
-
Zenith Alpha 2 Thoracic Endovascular Graft recall
FDA
· Cook Medical Incorporated · Class I
-
Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) recall
FDA
· Percussionaire Corporation · Class I
-
Automated Impella Controller (AIC), used for left heart support blood… recall
FDA
· Abiomed, Inc. · Class I
-
BD Alaris Pump Infusion Sets for the following reference numbers: C24101E… recall
FDA
· CareFusion 303, Inc. · Class I
-
NOxBOXi Nitric Oxide Delivery System recall
FDA
· Noxbox Ltd · Class I
-
NOxBOXi Nitric Oxide Delivery System recall
FDA
· Noxbox Ltd · Class I
-
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P recall
FDA
· Medline Industries, LP · Class I
-
MAGNETOM Vida Fit recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Vida (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio Dot Upgrade recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio Dot recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Verio recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Spectra as the following: 1. MAGNETOM Spectra recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra Fit BioMatrix recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra fit recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Skyra (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Prisma recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Lumina (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Connectom.X. Model Number: 11371480 recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
MAGNETOM Cima.X (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
BIOGRAPH One (DE) recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
Biograph mMR. Model Number: 10433372 recall
FDA
· Siemens Medical Solutions USA, Inc · Class I
-
Atlan Product Name: Atlan A350XL Model recall
FDA
· Draeger, Inc. · Class I
-
Atlan Product Name: Atlan A350 Model recall
FDA
· Draeger, Inc. · Class I
-
Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological… recall
FDA
· Medline Industries, LP · Class I
-
Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers… recall
FDA
· Medline Industries, LP · Class I
-
Sterile Medline Convenience Kits: 1) EXTREMITY PACK… recall
FDA
· Medline Industries, LP · Class I
-
Sterile Medline Convenience Kits: 1) MAJOR PACK L-F… recall
FDA
· Medline Industries, LP · Class I
-
Automated Impella Controller (AIC) with the below brands and product codes recall
FDA
· Abiomed, Inc. · Class I
-
Medline medical convenience kits labeled as: 1… recall
FDA
· Medline Industries, LP · Class I
-
Medline medical convenience kits labeled as: 1… recall
FDA
· Medline Industries, LP · Class I
-
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC… recall
FDA
· Max Mobility LLC · Class I
-
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use… recall
FDA
· Max Mobility LLC · Class I
-
Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use… recall
FDA
· Max Mobility LLC · Class I
-
3M Ranger Blood/Fluid Warming High Flow Set recall
FDA
· 3M Company · Class I
-
ViziShot 2FLEX. Single Use Aspiration Needle recall
FDA
· Olympus Corporation of the Americas · Class I
-
DLP Left Heart Vent Catheter Malleable body and vented connector… recall
FDA
· Medtronic Perfusion Systems · Class I