BEUDAMED
    170 results · 16ms · Sources: EU EUDAMED, US FDA

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    BF-MP60: OES Bronchofiberscope

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·March 8, 2022

    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·September 11, 2025

    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·September 11, 2025

    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·September 11, 2025

    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·September 11, 2025

    OES 4000 Hysteroscope, Model/Catalog Number: A4674A

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code HIH·April 18, 2024

    Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OE-001

    FDA Recall
    Open, Classified ·Dexcom, Inc.·Product code QBJ·January 27, 2025

    Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·June 8, 2023

    PENTAX Medical Video Colonoscope- Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastrointestinal tract Model: EC38-i20cL

    FDA Recall
    Open, Classified ·Pentax of America Inc·Product code PEA·January 29, 2025

    PENTAX Medical Video Upper GI Scope-Intended to provide optical visualization of (via a video monitor), and therapeutic access to the lower gastrointestinal tract Model: EG29-i20c

    FDA Recall
    Open, Classified ·Pentax of America Inc·Product code PEA·January 29, 2025

    Pentax Medical Video Processor- Intended to be used with PENTAX Medical endoscopes, monitors and other peripheral devices for endoscopic diagnosis, treatment, and video observation. Model: EPK-i8020c

    FDA Recall
    Open, Classified ·Pentax of America Inc·Product code PEA·January 29, 2025

    Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A

    FDA Recall
    Open, Classified ·Product code OES·May 28, 2026

    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) CATH PACK, Model Number DYNJ83105; b) TESIO, Model Number DYNJ83251; c) ANGIOGRAPHY PACK-LF, Model Number DYNJ83508; d) OR ANGIOGRAM PACK-LF, Model Number DYNJ83656; e) FERRELL-DUCAN ANGIO, Model Number DYNJ83696; f) ANGIO KIT PACK, Model Number DYNJ83746; g) M&E ARTERIOGRAM PK, Model Number DYNJ83815; h) ANGIOGRAPHY CV RAD PACK, Model Number DYNJ83918; i) ANGIO PACK, Model Number DYNJ83936; j) ARTERIOGRAM - SUMMIT PACK, Model Number DYNJ84040; k) ANGIO PACK, Model Number DYNJ84190; l) ANGIO, Model Number DYNJ902507C; m) ANGIO, Model Number DYNJ902507D; n) ANGIO, Model Number DYNJ905151B; o) PACK ANGIOPLASTY CV,8405, Model Number DYNJ906766B; p) (13) STC IVC FILTER/ANGIOGRAM, Model Number DYNJ908249A; q) OR ANGIOGRAM, Model Number DYNJ909267; r) RADIOLOGY PACK #108402-LF, Model Number DYNJVB1000; s) HYBRID OR PACK, Model Number SYNJ10303C

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OES·May 18, 2023

    Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ; 4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ; 5) ARTERIOGRAM PACK, Pack Number DYNJ53018; 6) CATH PACK , Pack Number DYNJ57729C ; 7) PEDS CATH PACK, Pack Number DYNJ66856; 8) PEDS CATH PACK, Pack Number DYNJ66856A ; 9) STEWARD ROCKLEDGE CATH RRS, Pack Number DYNJ81061A ; 10) CATH LAB PACK , Pack Number DYNJ84617; 11) UA/UV CATHETERIZATION TRAY, Pack Number UVT1190A

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OES·April 8, 2024

    Sterile Procedural Trays, labeled as the following: a. CARDIAC CATH PACK-LF; b. ANGIOGRAPHY-NS-LF; c. EP BASIC SET UP PACK; d. IMPLANT PACK-LF; e. PORT PACEMAKER INSERTION PACK; f. OPEN HEART PACK; g. LAP BASIN TRAY; h. ANGIO ACCESS; i. ANGIO

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OES·November 17, 2022

    Halyard IR ABCESS DRAINAGE PACK - Medical convenience kits Model Number: AVMD018

    FDA Recall
    Open, Classified ·AVID Medical, Inc.·Product code OES·September 20, 2024

    Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.

    FDA Recall
    Open, Classified ·AVID Medical, Inc.·Product code OES·March 13, 2026

    Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

    FDA Recall
    Open, Classified ·AVID Medical, Inc.·Product code OES·March 13, 2026

    Medline procedural kits labeled as: 1) PERIPHERAL ULTRASOUND CATHETER INSERTION, Pack Number MNS9865; 2) CIRCUMCISION TRAY, Pack Number CIT6715; 3) OSF SMMC CIRCUMCISION KIT, Pack Number CIT7095

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OES·April 8, 2024

    Halyard MANIFOLD CATH PACK - Medical convenience kits Model Number: VMED005-03

    FDA Recall
    Open, Classified ·AVID Medical, Inc.·Product code OES·September 20, 2024