device recall - Robuta Search

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=38881 Class 2 Device Recall Baxter Auto Syringe AS50 Infusion Pump device recall class baxter auto syringe https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=208755 Class 2 Device Recall Merit Medical device recall class merit medical https://trievrrecallmanagement.com/medical-device-recall-management-bedford-ma/ Medical Device Recall Management Bedford MA - recall management software services and solutions Sep 15, 2020 - Why Your Medical Device Company Needs to Be Using SaaS Recall Management Service Software medical device recall software services management bedford solutions https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=66343 Class 2 Device Recall PremierEdge REF MICROSURGICAL KNIFE 2.85mm Clear Cornea Knife device recall class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=194255 Class 2 Device Recall The CoolSculpting System device recall class coolsculpting system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=85926 Class 2 Device Recall SCORPIO NRG KNEE SYSTEM device recall class scorpio nrg knee https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=150044 Class 2 Device Recall TANDEM Bipolar Hip System device recall class tandem bipolar hip https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=142116 Class 2 Device Recall Contender Postop Knee Brace Full Foam device recall knee brace class contender postop https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218922 Class 2 Device Recall Cook Staged Extubation Set device recall class cook staged extubation https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=199910 Class 3 Device Recall CARDIOSAVE HYBRID device recall class hybrid https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=154793 Class 2 Device Recall Dressing Shldr XL device recall class dressing xl https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=219227 Class 2 Device Recall MiniMed 740G System device recall class minimed system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=45092 Class 1 Device Recall AccuChek device recall class accuchek https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=131660 Class 2 Device Recall PKG, PKG, HOOK SCISSORS device recall class pkg hook scissors https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218804 Class 2 Device Recall Olympus PKS Cutting Forceps, 5mm 33cm device recall cutting forceps class olympus pks https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=132898 Class 2 Device Recall System 6 Aseptic Housing device recall class system aseptic housing https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=161737 Class 2 Device Recall Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL device recall class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=193531 Class 2 Device Recall MEDLINE Polyurethane Foam Bedside Cleaning Kit device recall polyurethane foam class medline bedside https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=203672 Class 2 Device Recall Disposable SpetzlerMalis Bipolar forceps device recall class disposable bipolar forceps https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=82407 Class 2 Device Recall Stryker 100 mL AutoFuser PainPump device recall class stryker ml autofuser https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=181617 Class 2 Device Recall BioFlo and Xcela device recall class bioflo xcela https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=108570 Class 2 Device Recall Nexgen Complete Knee System device recall class nexgen complete knee https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=127033 Class 2 Device Recall BioGlue Surgical Adhesive (BioGlue) device recall class surgical adhesive https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=30982 Class 2 Device Recall ACE trochanteric nail systems device recall class ace nail systems https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=39868 Class 2 Device Recall P.F.C. device recall class p f https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=156508 Class 2 Device Recall 18 cm (7") PUR Smallbore Ext Set device recall class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=169170 Class 2 Device Recall Laparotomy Sponge device recall class laparotomy sponge https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=126900 Class 2 Device Recall Panda WallMount Infant Warmers, integrated with Nellcor SpO2 device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=173542 Class 1 Device Recall SHERPA NX ACTIVE GUIDING CATHETER device recall class sherpa nx active https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=96078 Class 2 Device Recall DEPUY ASR RESURFACING FEMORAL HEADS device recall depuy asr class resurfacing femoral https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=208020 Class 2 Device Recall Medline device recall class medline https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=88811 Class 2 Device Recall Single shot needle device recall single shot class needle https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=156760 Class 2 Device Recall Arrow Glide Thru PeelAway Sheath/Dilator Introducer device recall class arrow https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=151179 Class 2 Device Recall LOW PROFILE ABUTMENTS INTERNAL AND EXTERNAL CONNECTION internal and external device recall low profile class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=125015 Class 2 Device Recall InteGrip Acetabular Augment device recall class augment https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=109046 Class 2 Device Recall LUSTER HIP device recall class luster hip https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=209662 Class 2 Device Recall Medline device recall class medline https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=198103 Class 2 Device Recall Siemens, Atellica IM Folate, ADVIA Centaur Folate device recall siemens atellica class im folate https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=66946 Class 2 Device Recall UHR device recall class uhr https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=67260 Class 2 Device Recall TPS Drum device recall class tps drum https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=155726 Class 2 Device Recall Arrow Access Kit device recall class arrow access kit https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=166321 Class 2 Device Recall Affixus Hip Fracture Nail Left device recall hip fracture class nail left https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=168624 Class 2 Device Recall Philips Brilliance Big Bore Oncology brilliance big bore device recall class philips oncology https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=182740 Class 2 Device Recall IV Administration Set device recall iv administration class set https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=166859 Class 2 Device Recall Capnostream20 (US)M REFURBISHED device recall class us refurbished https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=206360 Class 2 Device Recall Exactech Equinoxe device recall class exactech equinoxe https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=171150 Class 2 Device Recall LW Scientific ZIP IQ Combo Centrifuge device recall lw scientific class zip iq https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=181830 Class 2 Device Recall NPWT 300cc Canister With Gel device recall class npwt canister gel https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=189254 Class 2 Device Recall Solex 7 Intravascular Heat Exchange Catheter Kit device recall heat exchange class solex https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=201376 Class 2 Device Recall Medline Probe Cover Kits device recall probe cover class medline kits https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=202670 Class 1 Device Recall HUDSON RCI Addipak device recall hudson rci class addipak https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=69690 Class 2 Device Recall Zimmer Spine Cyclone anterior cervical plate system anterior cervical plate device recall class zimmer https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=128607 Class 2 Device Recall Hitachi Echelon Oval MRI system device recall class hitachi echelon oval https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=191816 Class 2 Device Recall Helix Elite device recall class helix elite https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=88091 Class 2 Device Recall Stryker Xia Precision System device recall class stryker xia precision https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=124589 Class 2 Device Recall FREELOCK FEMORAL HIP FIXATION SYSTEM device recall class freelock femoral hip https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=131224 Class 2 Device Recall da Vinci Xi" Surgical System da vinci xi device recall class surgical system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=154548 Class 2 Device Recall da Vinci Xi EndoWrist Suction Irrigator da vinci xi device recall class suction irrigator https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=73745 Class 2 Device Recall GE Precision XR/a device recall class ge precision xr https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=180450 Class 2 Device Recall FOOTPRINT Ultra PH Suture Anchor 4.5 device recall suture anchor class footprint https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=139818 Class 2 Device Recall Sterile, GS0694 Robotic Lap surgical kit device recall class sterile robotic lap https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=154110 Class 2 Device Recall STAPLER,IS4000; da Vinci Xi EndoWrist Stapler Release Kit da vinci xi device recall https://beautifydata.com/us-fda/recalls/medical-device-recall-enforcement-per-firm-per-year-per-recall-id/naimco-inc-dba-richmar-inc/2013/z-0815-2013-cloth-electrodes-with-carbon-construction-p-n-201-1231-cat-nos-201-123-202-454-203-118-203-342-203-454-203-493-203-672-400-877-and-400-877-bjc-2-amp-quot-x-2-amp-quot-electrode-clot NAImco Inc dba Richmar Inc: Medical Device Recall in 2013 - (Recall #: Z-0815-2013) medical device recall detail. Product Description: Cloth electrodes with Carbon construction: P/N 201-1231, Cat Nos.: 201-123, 202-454, 203-118, 203-342,... medical device recall inc dba richmar https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=202727 Class 2 Device Recall nanoDot device recall class nanodot https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=110226 Class 2 Device Recall Universal Spinal System Lamina Hooks device recall class universal spinal system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=179806 Class 2 Device Recall Vaccess CT PowerInjectable Implantable Port device recall class ct implantable port https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=122177 Class 2 Device Recall VITROS Chemistry Products ECO2 Slides device recall class vitros chemistry products https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=141537 Class 1 Device Recall Optisure HV lead device recall class hv lead https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=197237 Class 2 Device Recall Philips Ingenia Elition X device recall class philips ingenia x https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=149604 Class 2 Device Recall cobas MODULAR PREANALYTICS system device recall class cobas modular preanalytics https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=180443 Class 2 Device Recall BIOMET Orthopedics device recall class biomet orthopedics https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=66338 Class 2 Device Recall 3.0mm Slit Knife for Eyemaxx device recall class slit knife https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=166903 Class 2 Device Recall Vanguard 360 Revision Knee System device recall revision knee class vanguard system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=73727 Class 2 Device Recall Digital Fluoroscopic Imaging System device recall fluoroscopic imaging class digital system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218642 Class 2 Device Recall MICS3 device recall class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=155738 Class 2 Device Recall Arterial Catheterization Kit device recall class arterial catheterization kit https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=128260 Class 2 Device Recall ACL TOP 300 CTS device recall class acl top cts https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=155275 Class 2 Device Recall MiniMed 640G device recall class minimed https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=139903 Class 3 Device Recall Alere Cholestech LDX Multianalyte Controls device recall cholestech ldx class alere multianalyte https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=208448 Class 2 Device Recall Nitro device recall class nitro https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=173644 Class 1 Device Recall SHERPA NX ACTIVE GUIDING CATHETER device recall class sherpa nx active https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=184599 Class 1 Device Recall ThermaCor device recall class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=139008 Class 2 Device Recall OPEN HEART PACK device recall open heart class pack https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=122164 Class 2 Device Recall VITROS Chemistry Products BUN/UREA Slides device recall class vitros chemistry products https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=35494 Class 2 Device Recall Kendall device recall class kendall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218685 Class 1 Device Recall TRUE METRIX PRO Professional Monitoring Blood Glucose System device recall true metrix https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=144633 Class 2 Device Recall Ossur Lil Angel Vest device recall class ossur lil angel https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=189266&ref=newyork.legalexaminer.com Class 2 Device Recall OPTETRAK Comprehensive Knee System device recall class comprehensive knee system https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=212591 Class 1 Device Recall ID Circuit device recall class id circuit https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=205135 Class 2 Device Recall Custom procedural convenience kits and trays device recall class custom procedural convenience https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=208151 Class 2 Device Recall Medline device recall class medline https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=30509 Class 2 Device Recall TDx/TDxFLx and TDxFLx Carbamazepine Reagents device recall class tdx carbamazepine reagents https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=206662 Class 1 Device Recall Boston Scientific Expo device recall boston scientific class expo https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=126202 Class 2 Device Recall PenAdapt"(PenAdapt is a TM of Buffalo Filter) device recall class https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=213568 Class 2 Device Recall SmartPath device recall class smartpath https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=163448 Class 2 Device Recall Kelyniam CSI device recall class csi https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=172100 Class 1 Device Recall SHERPA NX ACTIVE GUIDING CATHETER device recall class sherpa nx active https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=186697 Class 2 Device Recall Groshong NXT ClearVue Catheter device recall class nxt clearvue catheter https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=211664 Class 1 Device Recall PROPONENT DR device recall class proponent dr https://app.recallwire.com/ RecallWire | Medical Device Recall Management System Medical Device Recall Management System medical device recall management system