recall class - Robuta Search

https://mettrumclassaction.ca/index.html Mettrum Ltd. Medical Marijuana Recall Class Action medical marijuana recall class ltd action https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=167017 Class 2 Device Recall Ultrasonic Bronchoscope BFUC180F class device recall ultrasonic bronchoscope https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=152368 Class 2 Device Recall Minimal Access Attachment, BLACK MAX class device recall minimal access https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=209341 Class 2 Device Recall BVI CustomEyes Procedure Packs class device recall bvi procedure https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=219451 Class 2 Device Recall Paradigm REALTime Insulin Pump class device recall paradigm realtime https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=126895 Class 2 Device Recall Panda iRes Infant Warmers integrated with Nellcor SpO2 https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=198839 Class 2 Device Recall Leksell Stereotactic System class device recall stereotactic system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=196416 Class 2 Device Recall 3M SteriDrape class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=162074 Class 2 Device Recall ARROW, ARROWGARD AND ARROWGARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS... https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=197058 Class 2 Device Recall API INDUSTRIAL class device recall api industrial https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=94707 Class 1 Device Recall VITEK 2 Gram Negative Susceptibility Card, ASTN087 class device recall vitek https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=160188 Class 2 Device Recall VERSYS BEADED FULLCOAT BOWED REVISION HIP PROSTHESIS revision hip class device recall versys https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=188994 Class 2 Device Recall McKesson Lap Sponge class device recall mckesson lap https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=198966 Class 1 Device Recall Trilogy Evo Universal class device recall trilogy evo https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=180598 Class 2 Device Recall da Vinci Xi Surgical System da vinci xi class device recall surgical https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=200543 Class 1 Device Recall medtronic class device recall medtronic https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=82396 Class 2 Device Recall Stryker 550 mL AutoFuser PainPump class device recall stryker ml https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=33856 Class 2 Device Recall class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=149615 Class 2 Device Recall Basic Pack class device recall basic pack https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=148324 Class 2 Device Recall Covidien Valley Lab class device recall covidien valley https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=66623 Class 2 Device Recall Biomet RINGLOC Instrumentation Impactor Plate class device recall biomet instrumentation https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=69690 Class 2 Device Recall Zimmer Spine Cyclone anterior cervical plate system class device recall zimmer https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=106398 Class 2 Device Recall Irrigation Tray w/Bulb syringe class device recall irrigation tray https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=160457 Class 2 Device Recall Unifine Pentips 5mm x 31G pen needles class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=96145 Class 2 Device Recall DEPUY ASR XL ACETABULAR CUP SYSTEM (UNI FEMORAL) https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=202915 Class 2 Device Recall MEDLINE ReNewal class device recall medline renewal https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=181472 Class 2 Device Recall Ortho Clinical Diagnostics class device recall ortho clinical https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218331 Class 2 Device Recall Pelvic Reconstruction System (PRS) pelvic reconstruction class device recall system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=219078 Class 2 Device Recall BiDop 3 class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=67333 Class 1 Device Recall Dura Star class device recall dura star https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=80196 Class 2 Device Recall FreeStyle and FreeStyle Lite Blood Glucose Monitoring Test Strips blood glucose monitoring freestyle and https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=92504 Class 2 Device Recall Terumo Custom Kit class device recall terumo custom https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=166634 Class 2 Device Recall CLAMP STYLE CATHETER CONNECTOR 20GA LF class device recall clamp style https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=33362 Class 2 Device Recall class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=153107 Class 2 Device Recall Regard class device recall regard https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=67373 Class 1 Device Recall Dura Star class device recall dura star https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218799 Class 2 Device Recall Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=118918 Class 2 Device Recall NexGen Complete Knee Solution class device recall nexgen complete https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=184167 Class 3 Device Recall InTice" C Porous Ti Cervical Interbody System class device recall intice https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=128240 Class 2 Device Recall Stryker BAM (SHAPE) ARM, RIGHT class device recall stryker bam https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=178573 Class 2 Device Recall CenturionSuture Trays class device recall trays https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=198012 Class 2 Device Recall MEDLINE Surgical convenience kits class device recall medline surgical https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=141482 Class 2 Device Recall NxStage System One class device recall nxstage system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=202378 Class 2 Device Recall MEDICREA INTERNATIONAL S.A. class device recall international https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=148881 Class 2 Device Recall RadSuite class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=49757 Class 2 Device Recall Diagnostic Chemicals Limited diagnostic chemicals class device recall limited https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=188315 Class 2 Device Recall Zimmer class device recall zimmer https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=203491 Class 1 Device Recall Astral 100 and Astral 150 ventilators class device recall astral ventilators https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=209949 Class 2 Device Recall CADD class device recall cadd https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=52950 Class 2 Device Recall B Braun Thermodilution Right Heart Catheters b braun right heart class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=203676 Class 2 Device Recall Disposable SpetzlerMalis Bipolar forceps class device recall disposable bipolar https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=217917 Class 2 Device Recall Broviac class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=209054 Class 2 Device Recall Alcon Ophthalmic Knife class device recall alcon ophthalmic https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=96393 Class 2 Device Recall INTELLECT CRANIAL NAVIGATION SYSTEM SALES DEMO cranial navigation system sales class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=45844 Class 2 Device Recall Medtronic class device recall medtronic https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=156673 Class 2 Device Recall ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter... class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=94550 Class 2 Device Recall R3 Constrained Acetabular Liner class device recall constrained liner https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=107622 Class 2 Device Recall Terumo Advanced Perfusion System 1 perfusion system class device recall terumo https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=154711 Class 2 Device Recall Pressure Injectable MultiLumen Cental Venous Catheterization Kit class device recall pressure https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=181720 Class 2 Device Recall CALLOS BONE VOID FILLER, SKAFFOLD NEXT GENERATION BONE VOID FILLER,... class device recall callos https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=65397 Class 2 Device Recall Tucker Embryo Catheter class device recall tucker embryo https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=123818 Class 2 Device Recall SIGMA LCS HIGH PERFORMANCE" class device recall sigma lcs https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=164000 Class 2 Device Recall ARROW PICC Set class device recall arrow picc https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218298 Class 2 Device Recall Medline Convenience Kits class device recall medline convenience https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=88811 Class 2 Device Recall Single shot needle single shot class device recall needle https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=209388 Class 2 Device Recall BVI CustomEyes Procedure Packs class device recall bvi procedure https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=212782 Class 2 Device Recall Proxima Drape class device recall proxima drape https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=35884 Class 3 Device Recall class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=117106 Class 2 Device Recall Centricity Laboratory System class device recall centricity laboratory https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=188134 Class 2 Device Recall Cellex qSARSCov2 Antigen Rapid Test class device recall antigen rapid https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=137341 Class 2 Device Recall Beaver Visitec International, Inc class device recall beaver visitec https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=77508 Class 2 Device Recall Boston Scientific Stonetome Stone Removal Device boston scientific class device recall stone https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=142928 Class 2 Device Recall EndoVive 3s Low Profile Balloon Kits low profile class device recall balloon https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=92126 Class 2 Device Recall NEXGEN COMPLETE KNEE SOLUTION MIS TIBIAL COMPONENTS, LOCKING SCREW AND STEM... https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218613 Class 3 Device Recall Pacific Bathing Spa class device recall pacific bathing https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=200536 Class 1 Device Recall medtronic class device recall medtronic https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=173703 Class 1 Device Recall SHERPA NX ACTIVE GUIDING CATHETER class device recall sherpa nx https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=187586 Class 2 Device Recall Philips class device recall philips https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=217408 Class 1 Device Recall Vapor 2000 class device recall vapor https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=211821 Class 2 Device Recall Smaxel Fractional CO2 Laser class device recall smaxel fractional https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=183783 Class 2 Device Recall TWINFIX ULTRA PLLA HA 6.5MM W/ NEEDLES Absorbable Suture anchor https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=171233 Class 2 Device Recall CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM class device recall certain https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=107638 Class 2 Device Recall Fusio Liquid Dentin class device recall fusio liquid https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=25681 Class 2 Device Recall Ultracell class device recall ultracell https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=26458 Class 2 Device Recall CryoValve, Allograft class device recall allograft https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=30897 Class 2 Device Recall ACE trochanteric nail systems class device recall ace nail https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=104914 Class 2 Device Recall Heritage Labs Wellness Kits w/Purple Top, wellness kits class device recall heritage https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=91214 Class 2 Device Recall DePuy ASR 100 Acetabular Implant 44mm class device recall depuy asr https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=171794 Class 1 Device Recall Endoscopic Curved Intraluminal Stapler, 29 mm diameter, Model ECS29A https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=114817 Class 3 Device Recall Siemens ChekStix Positive and Negative Control Strips negative control class device recall siemens https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=194232 Class 2 Device Recall EEA Autosuture Circular Stapler class device recall eea circular https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218252 Class 2 Device Recall Philips Azurion systems recall philips class device systems https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=82390 Class 2 Device Recall Zimmer Alumina Ceramic Femoral Head alumina ceramic class device recall zimmer https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=151423 Class 2 Device Recall Arthex S3 Arm Sleeve Connector arm sleeve class device recall connector https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=105377 Class 2 Device Recall Siemens syngo Imaging XS, versions VA70A and VA70B Client/Server Installations https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=197992 Class 2 Device Recall SOMATOM go.Platform,go.Now,go.Up, go.All,... class device recall go platform https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=211737 Class 2 Device Recall Pediatric CystoUrethroscope class device recall pediatric https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=67102 Class 2 Device Recall Stryker Medical Epic II Critical Care Bed with Zoom Drive System; Model 2040. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=219029 Class 2 Device Recall XTANT MEDICAL Xpress Pedicle Screw System medical xpress pedicle screw class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=82584 Class 2 Device Recall Stryker Epic II critical care bed critical care class device recall stryker