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Contact a lawyer to see if you have a Kogalla Power Bank Recall Class Action Lawsuit. power bank recall class action lawsuit https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=127391 Class 2 Device Recall IntelliVue MX40 Wearable Patient Monitor in use with the Philips IntelliVue... https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=213345 Class 2 Device Recall LinkSymphoKnee class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=181708 Class 2 Device Recall CALLOS BONE VOID FILLER, SKAFFOLD NEXT GENERATION BONE VOID FILLER,... void filler class device recall callos https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=170557 Class 2 Device Recall CheckFlo Performer Introducer class device recall performer introducer https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=203296 Class 2 Device Recall Beckman Coulter DxI 9000 Access Immunoassay Analyzer beckman coulter class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=164015 Class 2 Device Recall VPS TipTracker Stylet Accessory class device recall vps stylet https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=33019 Class 2 Device Recall TPN compounder disposable valve set class device recall tpn disposable https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=87304 Class 2 Device Recall Outlook Pump IV Set w/Universal Spike Check Valve, 4 Ultrasite Inj Sites, 3... https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=127705 Class 2 Device Recall TECNIS CL class device recall tecnis https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=130773 Class 2 Device Recall Hospira class device recall hospira https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=73562 Class 2 Device Recall LifeStent FlexStar Stent System class device recall stent system https://www.pharmdata.co.uk/mhra_alert.php?id=5c1ff92350f5240f70d8be8a2e05b2cb Class 3 Medicines Recall: Theramex Ireland Ltd T/A Theramex HQ UK Ltd, AlfaD Capsules, EL (20) A/46... Read and respond to this pharmacy MHRA alert online with your PharmData account https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=208006 Class 1 Device Recall Plum A & Plum A3 Infusion Systems class device recall plum infusion https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=131407 Class 2 Device Recall Philips Healthcare recall philips class device healthcare https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=132781 Class 2 Device Recall Hudson RCI Humidifier Adaptor, 040. class device recall hudson rci https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=73908 Class 2 Device Recall Medtronic SynchroMed EL Programmable Pump class device recall medtronic el https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=202555 Class 2 Device Recall Airway Mobilescope class device recall airway mobilescope https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=218299 Class 2 Device Recall Medline Convenience Kits class device recall medline convenience https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=125116 Class 1 Device Recall ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port, 7.5, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=100603 Class 1 Device Recall Innova SelfExpanding Stent System class device recall innova stent https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=206265 Class 1 Device Recall Stay Safe Catheter Extension Sets and stay"safe/Luer Lock Adapter https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=125798 Class 1 Device Recall Hospira Acclaim Encore Infusion Pump class device recall hospira acclaim https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=141889 Class 3 Device Recall DrugSmart class device recall https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=85928 Class 2 Device Recall SCORPIO NRG KNEE SYSTEM class device recall scorpio nrg https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=114203 Class 2 Device Recall Remel X/pect Clostridium Difficile Toxin A/B (20 tests) https://news.pda.org/article/203093/class-2-device-recall-hiresolution-bionic-ear-system Class 2 Device Recall HiResolution Bionic Ear System Apr 28, 2026 - Date Initiated by Firm March 23, 2026 Product Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: ... class device recall bionic ear https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=165112 Class 2 Device Recall PROLENE Polypropylene Nonabsorbable Suture class device recall prolene polypropylene https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=187137 Class 2 Device Recall Pan Medical US/Zavation class device recall pan medical https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=122146 Class 2 Device Recall VITROS Chemistry Products ALB Slides class device recall chemistry products https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=43101 Class 2 Device Recall Sigma Pacemaker class device recall sigma pacemaker https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=175199 Class 2 Device Recall Paradigm Insulin Pump System insulin pump class device recall paradigm https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=195229 Class 2 Device Recall Exactech class device recall exactech https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=161948 Class 2 Device Recall class device recall