BEUDAMED
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    Excia Cemented Hip Stems, Size 12mm, Part Number: NJ312K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 17mm, Part Number : NJ317K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 14mm, Part Number : NJ314K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems ,Size 18mm, Part Number NJ318K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 13mm, Part Number : NJ313K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 16mm, Part Number NJ316K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 9mm, Part Number: NJ309K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 11mm, Part Number : NJ311K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 10mm, Part Number: NJ310K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 15mm, Part Number: NJ315K Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    AS VEGA SYSTEM® PS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 13, 2026

    AS VEGA SYSTEM® PS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 12, 2026

    KNEE ENDOPROSTHETICS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 12, 2026

    S4 POLYAXIAL SCREW 6.0X35MM

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code KWQ·June 1, 2007

    S4 SET SCREW NEW VERSION

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code KWP·May 10, 2007

    EXCIA PLASMAPORE-UCAP 8/10 SIZE 13MM

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code JDI·June 1, 2007

    S4 SET SCREW NEW VERSION

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code KWP·May 30, 2007

    CASPAR DISTR PIN 14 MMSTER

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code LXH·April 14, 2007

    S4 SET SCREW NEW VERSION

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, INC.·Product code KWP·May 30, 2007

    S4 POLYAXIAL SCREW 6.0X40MM

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, INC.·Product code KWP·February 22, 2007