-
BD Pyxis Mini Main recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis Anesthesia Station 4000 recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis Anesthesia Station ES recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis MedStation ES recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis MedStation 4000 recall
FDA
· CareFusion 303, Inc. · Class II
-
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2))… recall
FDA
· Bayer Medical Care, Inc. · Class II
-
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed… recall
FDA
· Daavlin Distributing Company · Class II
-
Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall
FDA
· Shimadzu Medical Systems · Class II
-
Arvis Hip & Knee 2.0 Instrument Set recall
FDA
· Kico Knee Innovation Company · Class II
-
Arvis Hip & Knee 3.0 Instrument Set recall
FDA
· Kico Knee Innovation Company · Class II
-
Philips Azurion 7M20, Model Numbers: 722079… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 7M12, Model Numbers: 722078… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 7B20/15, Model Numbers: 722068… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 7B12/12, Model Numbers: 722067… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 3M15, Model Numbers: 722064… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Philips Azurion 3M12, Model Numbers: 722063… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus… recall
FDA
· Advanced Bionics, LLC · Class II
-
Neptune Smart Docking Station (120V) recall
FDA
· Stryker Corporation · Class II
-
Covidien EndoStitch" Polysorb Single Use Loading Unit recall
FDA
· Covidien, LP · Class II
-
CASE v7.0 Cardiac Testing System Model no recall
FDA
· GE Medical Systems Information Technologies Inc · Class II
-
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits:… recall
FDA
· B Braun Medical Inc · Class I
-
Spinocan Spinal Needle procedure kits: Material Description (Material… recall
FDA
· B Braun Medical Inc · Class I
-
Spinal Needle procedure kits: Material Description (Material Number) 24GA… recall
FDA
· B Braun Medical Inc · Class I
-
PhaseOne Antimicrobial Solution, Model recall
FDA
· Oculus Technologies of Mexico, S.A. de C.V. · Class II
-
The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS) recall
FDA
· Fresenius Kabi USA, LLC · Class II
-
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr recall
FDA
· Covidien, LP · Class II
-
Covidien Mon-a-Therm General Purpose Temperature Probe recall
FDA
· Covidien, LP · Class II
-
Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM recall
FDA
· Covidien, LP · Class II
-
B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC. Product Name: CESK RIVERSIDE HEALTH SYSTEM Model recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID… recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP… recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC. Product Name: BPSK, BLOCKJOCKS TRAY Model recall
FDA
· B Braun Medical Inc · Class II
-
B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model recall
FDA
· B Braun Medical Inc · Class II
-
Exacta Mix Product Name: Vented Micro-Volume Inlet Model recall
FDA
· Baxter Healthcare Corporation · Class II
-
COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula recall
FDA
· Covidien, LP · Class II
-
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in… recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in recall
FDA
· Becton Dickinson & Co. · Class I
-
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004 recall
FDA
· Fresenius Kabi USA, LLC · Class I
-
LVP software of the Ivenix Infusion System (IIS) recall
FDA
· Fresenius Kabi USA, LLC · Class I
-
Pediatric care bed recall
FDA
· Kayserbetten Gmbh & CO. Kg · Class I
-
Atlan A350XL. Model Number: 8621600. anesthesia workstation recall
FDA
· Draeger, Inc. · Class I
-
Atlan A350. Model Number: 8211500. anesthesia workstation recall
FDA
· Draeger, Inc. · Class I
-
ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model… recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system recall
FDA
· Siemens Medical Solutions USA, Inc · Class II
-
Medline medical convenience kit labeled as EYE TRAY-LF… recall
FDA
· Medline Industries, LP · Class II
-
Allura system recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion system recall
FDA
· Philips Medical Systems Nederland B.V. · Class II