BEUDAMED
    4,541 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ATTUNE PS FB INSRT SZ 6 5MM

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code NJL·January 21, 2022

    MAIN ASSEMBLY, BLS, ZOLL AED 3, JAPANESE JRC

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 23, 2024

    MAIN ASSEMBLY, BLS, ZOLL AED 3, JAPANESE JRC

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 15, 2025

    SYRINGE 150 UL

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JRC·May 14, 2019

    SYRINGE 150 UL

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JRC·January 29, 2019

    SYRINGE 150 UL

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JRC·June 2, 2017

    SYRINGE 150 UL

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JRC·May 14, 2019

    RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surface of the Distal Stem is protected during proximal preparation.

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code KWA·June 3, 2014

    RECLAIM DISTAL TAPERED, Angled Distal Stem, various sizes. Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surface of the Distal Stem is protected during proximal preparation.

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code KWA·June 3, 2014

    RECLAIM DISTAL TAPERED Distal Stem, various sizes. Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surface of the Distal Stem is protected during proximal preparation.

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code KWA·June 3, 2014

    ATTUNE PS FB INSRT SZ 8 5MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·September 17, 2020

    KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·DEPUY SYNTHES·Product code JWH·April 24, 2025

    KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·DEPUY SYNTHES·Product code JWH·April 24, 2025

    MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000, 136342000, 136343000, 136344000, 136345000, 136346000, 136347000, 136348000, 136349000, 136350000, 136351000, 136352000, 136353000, 136354000, 136356000, 136358000, 136360000

    FDA Recall
    Open, Classified ·DePuy Orthopaedics, Inc.·Product code LZY·May 18, 2022

    PANTHER SYSTEM

    FDA Adverse Event
    Malfunction ·HOLOGIC, INC.·Product code MKZ·March 3, 2017

    SIGMA STAB GVF INS 2.5 10MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 4, 2021

    ATTUNE CR FEM TRIAL SZ 5 RT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·November 13, 2025

    ATTUNE CR FEM TRIAL SZ 6 RT

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code HWT·October 10, 2025

    HP UNI INS SZ3 7MM RMLL AOX

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HRY·December 12, 2025

    ATTUNE PS FEM TRIAL SZ 6 LT

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code HWT·April 9, 2024