Medical Device Recall Search

Recall Search

Medical Device Recall Search

Search live FDA recall data for medical devices. Enter a device type, brand name, or body area. Results come directly from the FDA's device recall database, updated continuously.

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1583 results for “hip”

  • G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in hip arthroplasty

    Recalling firm
    Zimmer, Inc.
    Status
    Open, Classified
    Date initiated
    2022-08-25
    Reason for recall
    The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner wall could potentially crack during transit. Potential risks include non-clinically or clinically significant extension of surgery, or infection leading to surgical intervention.

  • Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with th…

    Recalling firm
    Depuy Orthopaedics, Inc.
    Status
    Terminated
    Date initiated
    2010-06-15
    Reason for recall
    Firm discovered that some of their straight broach handles are experiencing early failure due to a weakened handle locking mechanism (Leaf Spring).

  • Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cup 46 mm cup Ref.: 74120146. Hip implant component.

    Recalling firm
    Smith & Nephew Inc
    Status
    Terminated
    Date initiated
    2007-07-12
    Reason for recall
    The carton label may not reflect the correct size of the acetabular cup.

  • Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cup, 44 mm cup Ref.: 74120144. Hip implant component.

    Recalling firm
    Smith & Nephew Inc
    Status
    Terminated
    Date initiated
    2007-07-12
    Reason for recall
    The carton label may not reflect the correct size of the acetabular cup.

  • Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cup, 46 mm cup Ref.: 74120146. Hip implant component.

    Recalling firm
    Smith & Nephew Inc
    Status
    Terminated
    Date initiated
    2007-07-12
    Reason for recall
    The carton label may not reflect the correct size of the acetabular cup.

  • Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cup, 48 mm cup Ref.: 74120148. Hip implant component.

    Recalling firm
    Smith & Nephew Inc
    Status
    Terminated
    Date initiated
    2007-07-12
    Reason for recall
    The carton label may not reflect the correct size of the acetabular cup.

  • Stryker Navigation System - Hip Module Patient Tracker, green; Model 6007-005-000.

    Recalling firm
    Stryker Instruments, Instruments Div.
    Status
    Terminated
    Date initiated
    2004-07-14
    Reason for recall
    The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.

  • Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cup, 50 mm cup Ref.: 74120150. Hip implant component.

    Recalling firm
    Smith & Nephew Inc
    Status
    Terminated
    Date initiated
    2007-07-12
    Reason for recall
    The carton label may not reflect the correct size of the acetabular cup.

  • Stryker Navigation System - Hip Module Patient Tracker, blue; Model 6007-010-000.

    Recalling firm
    Stryker Instruments, Instruments Div.
    Status
    Terminated
    Date initiated
    2004-07-14
    Reason for recall
    The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.

  • Smith + Nephew, Birmingham Hip Resurfacing, Acetabular Cup, 52 mm cup Ref.: 74120152. Hip implant component.

    Recalling firm
    Smith & Nephew Inc
    Status
    Terminated
    Date initiated
    2007-07-12
    Reason for recall
    The carton label may not reflect the correct size of the acetabular cup.