BEUDAMED
    21 results · 12ms · Sources: EU EUDAMED, US FDA

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    B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.

    FDA Recall
    Open, Classified ·B Braun Medical Inc·Product code FJK·March 19, 2026

    REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest or Jadk FM-5 barcode reader component.

    FDA Recall
    Open, Classified ·Cellavision AB Forskningsbyn Ideon Scheelevagen 19a Lund Sweden·Product code JOY·October 8, 2025

    STREAMLINE BLOODLINE LONG VERSION, FMC-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095L

    FDA Recall
    Open, Classified ·B Braun Medical Inc·Product code FJK·August 15, 2024

    SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095

    FDA Recall
    Open, Classified ·B Braun Medical Inc·Product code FJK·August 15, 2024

    Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that utilizes Apple iOS 17.4 and Apple iOS 17.5, a component of the Arial Emergency and Nurse Call System.

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·April 11, 2024

    ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 REF ASK-04020-EUH2 UDI code: (01)10801902213379(17)270731(11)251218(10)33F25J0869 REF ASK-04020-FMC UDI code: (01)10801902212099(17)270731(11)251218(10)33F25J0870 REF ASK-04020-MMC UDI code: (01)10801902117769(17)271130(11)251211(10)33F25J0880 The Arrow Arterial Catheterization Device permits access to the peripheral arterial circulation or to other small vessels.

    FDA Recall
    Open, Classified ·ARROW INTERNATIONAL, LLC·Product code OFB·March 11, 2026

    AirTouch F20 Full Face Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    AirFit F20 Full Face Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    AirFit N10 Nasal Masks and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    AirFit F30i Full Face Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    AirFit F30 Full Face Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    AirFit N20 Nasal Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    AirTouch N20 Nasal Mask and User Guide

    FDA Recall
    Open, Classified ·Product code BZD·November 20, 2023

    Medline Leg bag, REF DYND12578

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code FAQ·October 19, 2023

    Medline Leg bag, REF DYND12574

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code FAQ·October 19, 2023

    Medline Leg bag, REF URO12573

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code FAQ·October 19, 2023

    Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities Part number: 00880000010

    FDA Recall
    Open, Classified ·Zimmer Surgical Inc·Product code GFD·September 5, 2023

    CareLink Personal Software Therapy Management Software Tool for Diabetes CareLink System Therapy Management Software Tool for Diabetes Software Uploader versions: 3.1.5.000 3.1.2.000

    FDA Recall
    Open, Classified ·Medtronic Inc.·Product code MDS·November 12, 2020

    Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack Model/Catalog Number: STP-AT-012 Software Version: N/A Product Description: Dexcom G7 US Retail Sensor/Transmitter 1-pack Component: Dexcom G7 Continuous Glucose Monitoring System

    FDA Recall
    Open, Classified ·Dexcom, Inc.·Product code QBJ·May 27, 2026

    Procedure packs: (1) Presource PBDS, Cat. PGMHSUESR, Southeast Hospital MHHS, Kit, Set Up No Drape, SE, Sterile; (2) Presource PBDS Cat. PGVGLBP20, Parkview Medical Center, Kit, Lap Chole, Sterile; (3) Presource PBDS Cat. PG63CCC31, USPI Christ Hosp Spine Srgry C, Kit, Basic, Sterile; (4) Presource PBDS Cat. PG63CCC34, USPI Christ Hosp Spine Srgry C, Kit, Basic, Sterile; (5) Presource Robotic Module Pack, Cat. SBAOCRBENF, Englewood Hospital and Medical, Sterile; (6) Presource Robotic Module Pack, Cat. SBAOCRBEN8, Englewood Hospital and Medical, Sterile; (7) Presource FMC Liver Resection Pack, Cat. SBA30MJCHH, AHS Calgary Zone, Sterile; (8) Presource ALIF Pack, Cat. SBA41ALFME, USPI Baylor Med Ctr at Fri, Sterile; (9) Presource ACDF Pack, Cat. SBA44ACWBF, Webster Surgical Specialty Hos, Sterile; (10) Presource Lap Chole Pack, Cat. SBA54LADNA, USPI Paso Del Norte Srgry Ctr, Sterile; (11) Presource Lap Chole Pack, Cat. SBA54LADN3, USPI Paso Del Nrte Srgry Ctr, Sterile; (12) Presource Salle Hybride Ensemble, Cat. SCV30THLHA, Inst Univ Cardio ET Pneumo, Sterile; (13) Presource AMB Perc Pack, Cat. SMA57PR00B, Oregon Health Science Universi, Sterile; (14) Presource KP Vacaville Lami Pack, Cat. SNE69LPKVB, KP Vacaville, Sterile; (15) Presource Kyphoplasty Pack, Cat. SOP26KPMHB, Moffitt Cancer Center, Sterile; (16) Presource Percutaneous Nephro Pack, Cat. SOT30PELCA, Lakeridge Health Corporation, Sterile; and (17) Presource PBDS Infection Control Turnover Kit, Cat. ORC511687B, Sequoia Surgery Center LLC, Sterile.

    FDA Recall
    Open, Classified ·Cardinal Health 200, LLC·Product code LRO·August 16, 2023