• À propos de cette base de données
  • Comment utiliser cette base de données
  • Téléchargez les données
  • FAQ
  • Crédits
Mode Liste Mode Grille
  • Dispositif médical 1211
  • Fabricant 31827
  • Événement 5885
  • Implant 4142
Synex II Modular Vertebral Body Replacement System
  • Modèle / numéro de série
  • Classification du dispositif
    Orthopedic Devices
  • Dispositif implanté ?
    Yes
  • Description du dispositif
    Non-active implants
  • Manufacturer
    Synthes
  • 1 Event
    • Avis De Sécurité sur Synex II Modular Vertebral Body Replacement System
femoral neck component
  • Modèle / numéro de série
  • Classification du dispositif
    Orthopedic Devices
  • Dispositif implanté ?
    Yes
  • Description du dispositif
    Non-active implants - bone surgery
  • Manufacturer
    MicroPort Orthopedics
  • 1 Event
    • Avis De Sécurité sur femoral neck component
the Oasys Midline Plates
  • Modèle / numéro de série
  • Classification du dispositif
    Orthopedic Devices
  • Dispositif implanté ?
    Yes
  • Description du dispositif
    Non-active implants - bone surgery
  • Manufacturer
    STRYKER
  • 2 Events
    • Avis De Sécurité sur the Oasys Midline Plates
    • Avis De Sécurité sur the Oasys Midline Plates
Comprehensive Reverse Shoulder Tray
  • Modèle / numéro de série
  • Classification du dispositif
    Orthopedic Devices
  • Dispositif implanté ?
    Yes
  • Description du dispositif
    Non-active implants - bone surgery
  • Manufacturer
    Zimmer Biomet
  • 1 Event
    • Avis De Sécurité sur Comprehensive Reverse Shoulder Tray
Device Recall The HemiCAP Contoured Articular Prosthetic
  • Modèle / numéro de série
    Catalog Number: 8135-1875 Part Number: 3135-1875
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
  • Description du dispositif
    Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number: 8135-1875 Part Number: 3135-1875. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
  • Manufacturer
    Arthrosurface, Inc.
  • 1 Event
    • Rappel de Device Recall The HemiCAP Contoured Articular Prosthetic
Device Recall The HemiCAP Contoured Articular Prosthetic
  • Modèle / numéro de série
    Catalog Number: 8156-0032, Part Number: 156-0032
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
  • Description du dispositif
    Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component; Catalog Number: 8156-0032, Part Number: 156-0032. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
  • Manufacturer
    Arthrosurface, Inc.
  • 1 Event
    • Rappel de Device Recall The HemiCAP Contoured Articular Prosthetic
Device Recall Osteobond Copolymer Bone Cement
  • Modèle / numéro de série
    PMA #N17755, decision date 5/17/1976, reclassified 10/14/1999. Class II device; D033511, Item No. 00-1101-012-00; lot 62849791, 14D0809, Manufactured between 9/11/2014-10/6/2014; EXP date: 4/30/2017
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Distributed to MI, KS, and CA.
  • Description du dispositif
    Osteobond Bone Cement || Bone cement monomer is kitted with bone cement powder to create a cement mantle for orthopedic implants.
  • Manufacturer
    Zimmer, Inc.
  • 1 Event
    • Rappel de Device Recall Osteobond Copolymer Bone Cement
Device Recall Persona Cemented Tibial Broach Inserter/Extractor
  • Modèle / numéro de série
    Item: 42-5399-023-00 Lots: 62072307 62072565 62085420 62192754
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Distributed in the states of MN; NJ; NC; PA; AL; MI; OR; FL; OH; CO; IL and CA, and the countries of Australia, India, UAE, Germany, and Italy.
  • Description du dispositif
    Persona Cemented Tibial Broach Inserter/Extractor. || The Persona Cemented Tibial Broach Inserter/Extractor Handle is a Use sterilizable instrument intended for use In multiple TKA procedures. The Persona Surgical Technique indicates that the Persona Cemented Tibial Broach Inserter/Extractor Handle is intended to broach the proximal tibia in preparation for the full seating of the tibial implant.
  • Manufacturer
    Zimmer, Inc.
  • 1 Event
    • Rappel de Device Recall Persona Cemented Tibial Broach Inserter/Extractor
Device Recall Sirius Polish Cemented Stem 34B
  • Modèle / numéro de série
    Sirius Polish Cemented Stem 348 Catalog Number: 51-199333 Lot Number Identification: 024320
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Foreign Distribution in China and Australia only.
  • Description du dispositif
    Device Brand Name: Sirius Polish Cemented Stem 34B || Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, cemented || Device Common Name: Sirius Femoral Stem || The Biomet's Sirius Femoral Hip Stem is a double-tapered, highly polished cemented hip stem, designed for either primary or revision surgery. A distal centralizer is provided for optimal placement within the femoral canal. The system is used with Type 1 taper modular heads and compatible acetabular shells/liners and screws to provide a total hip replacement system.
  • Manufacturer
    Biomet, Inc.
  • 1 Event
    • Rappel de Device Recall Sirius Polish Cemented Stem 34B
Device Recall Sirius Polish Cemented Stem 34B
  • Modèle / numéro de série
    Sirius Polish Cemented Stem 38C Catalog Number: 51-199335 Lot Number Identification: 141680, 180920
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Foreign Distribution in China and Australia only.
  • Description du dispositif
    Sirius Polish Cemented Stem 38C || Catalog Number: 51-199335 || Lot Number Identification: 141680, 180920 || The Biomet's Sirius Femoral Hip Stem is a double-tapered, highly polished cemented hip stem, designed for either primary or revision surgery. A distal centralizer is provided for optimal placement within the femoral canal. The system is used with Type 1 taper modular heads and compatible acetabular shells/liners and screws to provide a total hip replacement system.
  • Manufacturer
    Biomet, Inc.
  • 1 Event
    • Rappel de Device Recall Sirius Polish Cemented Stem 34B
Device Recall SolitaireC Cervical Spacer System
  • Modèle / numéro de série
    Part number 14-531593 Part number 14-531594  Catalog number Lot Number 14-531593 N23597  14-531594 N23599
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    US Nationwide Distribution.
  • Description du dispositif
    Solitaire-C Cervical Spacer System || a) 14-531593 Drill/Awl Sleeve || b) 14-531594 Spring-Loaded Drill/Awl Sleeve || Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental fixation.
  • Manufacturer
    Ebi, Llc
  • 1 Event
    • Rappel de Device Recall SolitaireC Cervical Spacer System
Device Recall BIOLOX delta TS Ceramic Femoral Head Articul/eze 12/14 36mm 12
  • Modèle / numéro de série
    Lot 7928614 CATALOG NO. : 1365-36-740 Barcode GTIN: 10603295033684
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Distributed in the states of WV, AZ, and AL, and the countries of Germany, and Finland.
  • Description du dispositif
    Ceramic Femoral Head. || Intended for use in total hip arthroplasty applications to replace the articular surface of the femoral head in primary hip surgery and for the salvage of a failed previous hip surgery.
  • Manufacturer
    DePuy Orthopaedics, Inc.
  • 1 Event
    • Rappel de Device Recall BIOLOX delta TS Ceramic Femoral Head Articul/eze 12/14 36mm 12
Device Recall Trilogy Bone Screws
  • Modèle / numéro de série
    Item Number Lot Number 00-6250-065-35 62748089 00-6250-065-35 62754329 00-6250-065-35 62793494 00-6250-065-35 62793495 00-6250-065-35 62793501 00-6250-065-35 62793502 00-6250-065-35 62793503 00-6250-065-35 62813612 00-6250-065-35 62813613 00-6250-065-25 62784617 00-6250-065-25 62784618 2 00-6250-065-25 62784619 00-6250-065-25 62784621 00-6250-065-25 62784622 00-6250-065-25 62818701 00-6250-065-25 62818702 00-6250-065-25 62818703 00-6250-065-25 62818707 00-6250-065-25 62818709 00-6250-065-25 62818710 00-6250-065-25 62825611 00-6250-065-25 62836984
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA (nationwide) and Internationally to Canada Australia Brazil Chile China Colombia Japan Malaysia Singapore South Korea Taiwan Albania Austria Belgium Bulgaria Canary Islands Czech Republic Denmark Egypt Finland France Germany Greece Hungary Ireland Italy Netherlands Norway Poland Portugal Russia Saudi Arabia Serbia Slovakia South Africa Spain Sweden Switzerland Turkey and United Kingdom.
  • Description du dispositif
    Bone Screw, self-tapping || The Trilogy shells are available in three configurations; uni, multi, and cluster-holed. The multi and cluster-holed shells allow for the use of screws to provide additional fixation and security, particularly in those case where acetabular bone stock is deficient. The Trilogy Acetabular System is indicated for either cemented or uncemented use in skeletally mature individuals undergoing primary or revision surgery for rehabilitating hips damaged as a result of noninflammatory degenerative joint disease (NIDJD) or its composite diagnoses of osteoarthritis, avascular necrosis, protrusio acetabuli, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant.
  • Manufacturer
    Zimmer Manufacturing B.V.
  • 1 Event
    • Rappel de Device Recall Trilogy Bone Screws
Device Recall Timberline Anchored Lateral Retractable Drill
  • Modèle / numéro de série
    Model 8630-0102 Anchored Lateral Retractable Drill lot TU00049: February 25, 2013 and TU00155: July 31, 2013
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Distributed in PR and the states of NY, AZ, TN, TX, and CA.
  • Description du dispositif
    Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. || Timberline Anchored Lateral Retractable Drills are used with the Timberline MPF System to establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae.
  • Manufacturer
    Biomet Spine, LLC
  • 1 Event
    • Rappel de Device Recall Timberline Anchored Lateral Retractable Drill
Device Recall Timberline Anchored Lateral Variable Retractable Sleeve
  • Modèle / numéro de série
    Model 8630-0204 Lots TU00052, TU00052A, and TU00117
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    US Distribution to states of: AZ, CA, NY, TN, and TX including PR.
  • Description du dispositif
    Timberline Anchored Lateral Variable Retractable Sleeve LITPCR8600-2101-07, Model No. 86300204 || Timberline Anchored Lateral Variable Retractable Sleeves (the Sleeves) are used with the Timberline MPF System to help establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae.
  • Manufacturer
    Biomet Spine, LLC
  • 1 Event
    • Rappel de Device Recall Timberline Anchored Lateral Variable Retractable Sleeve
Device Recall Timberline Anchored Lateral Retractable Sleeve
  • Modèle / numéro de série
    LOT Numbers: TU00053A, TU00053B and TU00118 Product Code: 86300205
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    US Distribution to states of: AZ, CA, NY, TN and TX including PR.
  • Description du dispositif
    Timberline Anchored Lateral Fixed Retractable Sleeve Model No. 8630-0205. Timberline Anchored Lateral Fixed Retractable Sleeves are used with the Timberline MPF System to help establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae. The Timberline Retractable Drill and the Timberline Retractable Awl fit within this Sleeve. || Spinal Surgical Device.
  • Manufacturer
    Biomet Spine, LLC
  • 1 Event
    • Rappel de Device Recall Timberline Anchored Lateral Retractable Sleeve
Device Recall EXp Tibial Insert
  • Modèle / numéro de série
    part numbers SC3425 and SC3453, with lot numbers:28592-103112 28593-102412 28602-110112 28603-110112 28613-110112 28617-110112 28618-110112 28622-112812 28623-112812 28624-112812 31031-121013 31033-121013 31040-121013 31249-022514 31261-020414 28592-103112 28593-102412 28598-111412 28599-111412 28602-110112 28603-110112 28607-111912 28613-110112 28617-110112 28618-110112 28622-112812 28623-112812 28624-112812 31029-120913 31040-121013 31043-120913 31243-022414 31244-022414 31249-022514 31252-021314 31255-020414 31261-020414 32083-080714 31028-120913 31031-121013 31032-121013 31033-121013 31042-121013 31044-120913 31243-022414 31244-022414 31245-022414 31252-021314 31255-020414 31261-020414 31263-021314 31264-031114 31265-031114 31266-031114 28592-103112 28593-102412 28598-111412 28599-111412 28602-110112 28603-110112 28607-111912 28613-110112 28617-110112 28618-110112 28622-112812 28623-112812 28624-112812 31029-120913 31034-120913 31040-121013 31043-120913 31044-120913 31249-022514 31255-020414 32083-080714 28592-103112 28593-102412 28598-111412 28599-111412 28602-110112 28603-110112 28607-111912 28613-110112 28617-110112 28618-110112 28622-112812 28623-112812 28624-112812 31028-120913 31029-120913 31031-121013 31032-121013 31033-121013 31034-120913 31037-121013 31040-121013 31042-121013 31044-120913 31243-022414 31244-022414 31245-022414 31249-022514 31252-021314 31255-020414 31261-020414 31263-021314 31265-031114 32081-080714 28592-103112 28593-102412 28598-111412 28599-111412 28602-110112 28603-110112 28613-110112 28622-112812 28623-112812 28624-112812 31034-120913 28599-111412 28617-110112 31028-120913 31032-121013 31042-121013 31044-120913 31243-022414 31244-022414 31245-022414 31249-022514 31251-022514 31252-021314 31255-020414 31261-020414 31263-021314 31264-031114 31265-031114 31266-031114 28618-110112 28592-103112 28598-103112 28599-111412 28602-110112 28603-110112 28607-111912 28613-110112 28617-110112 28618-110112 28622-112812 28623-112812
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    TX, MD, IN, KS, CA, PA, GA, WA, NY, IL.
  • Description du dispositif
    EXp Tibial Insert ; Intended Use of Device(s): The Proven Gen-Flex Total Knee System is intended for: a. Total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis, and/or post-traumatic degenerative problems; and b. Revision of failed previous reconstructions where sufficient bone stock and soft tissue integrity are present.
  • Manufacturer
    Stelkast Co
  • 1 Event
    • Rappel de Device Recall EXp Tibial Insert
Device Recall Stryker Orthopedics
  • Modèle / numéro de série
    510K 983382  Lot code 49073501
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution including NY, OH, PA, and TX.
  • Description du dispositif
    Trident PSL HA Solid Back 50 mm || Includes Dome Hole Plug || Ref 540-11-50E || Intended for cementless application in a total hip arthroplasty procedure. This system is a two piece ( a shell and a liner) design that is assembled during surgery. The shell is press-fit into the patients prepared acetabulum and a linger (polyethylene or alumina ceramic) is then locked into the shell. The femoral head component of the total hip system articulates with the acetabular liner.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
  • 1 Event
    • Rappel de Device Recall Stryker Orthopedics
Device Recall Zimmer PERSONA
  • Modèle / numéro de série
    Item No. 42-5299-001-00 Affected Lots: 56572679; 56573170; 56574318; 56575056; 56572918; 56573378; 56574538; 56575057; 56572975; 56573379; 56574540; 56575058; 56572978; 56574123; 56574618; 56575059; 56572981; 56574124; 56574619; 56575060; 56572982; 56574223; 56574620; 56575061; 56573071; 56574291; 56574629; 56575062; 56573115; 56574292; 56574630; 56575065; 56573116; 56574316; 56574631; 56575080; 56573154; 56574317; 56575018
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide distribution: US nationwide, including Puerto Rico, South Korea, Singapore, Dominican Republic, Canada, Japan, and Germany.
  • Description du dispositif
    Zimmer PERSONA Tibial Articular Surface Inserter; Item # 42-5299-001-00. Manual surgical instrument for knee arthroplasty (orthopedic).
  • Manufacturer
    Zimmer, Inc.
  • 1 Event
    • Rappel de Device Recall Zimmer PERSONA
Device Recall PERSONA
  • Modèle / numéro de série
    Persona (TASP) Tibial Articular Surface Provisional Shim, all sizes and Lots Catalog Number: 42-5279-002-00 thru 42-5279-009-04: 42-5279-002-00 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, CD, 10mm; 42-5279-002-02 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, CD, 12mm; 42-5279-002-04 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, CD, 14mm; 42-5279-004-00 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, EF, 10mm; 42-5279-004-02 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, EF, 12mm; 42-5279-004-04 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, EF, 14mm; 42-5279-006-00 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, GH, 10mm; 42-5279-006-02 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, GH, 12mm; 42-5279-006-04 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, GH, 14mm; 42-5279-008-00 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, J, 10mm; 42-5279-008-02 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, J, 12mm; 42-5279-008-04 All Lots Persona Constrained TASP (Tibial A/S Prov.) Shim, J, 14mm; 42-5279-003-00 All Lots Persona TASP (Tibial A/S Provisional) Shim, CD, 10mm; 42-5279-003-01 All Lots Persona TASP (Tibial A/S Provisional) Shim, CD, 11mm; 42-5279-003-02 All Lots Persona TASP (Tibial A/S Provisional) Shim, CD, 12mm; 42-5279-003-03 All Lots Persona TASP (Tibial A/S Provisional) Shim, CD, 13mm; 42-5279-003-04 All Lots Persona TASP (Tibial A/S Provisional) Shim, CD, 14mm; 42-5279-005-00 All Lots Persona TASP (Tibial A/S Provisional) Shim, EF, 10mm; 42-5279-005-01 All Lots Persona TASP (Tibial A/S Provisional) Shim, EF, 11mm; 42-5279-005-02 All Lots Persona TASP (Tibial A/S Provisional) Shim, EF, 12mm; 42-5279-005-03 All Lots Persona TASP (Tibial A/S Provisional) Shim, EF, 13mm; 42-5279-005-04 All Lots Persona TASP (Tibial A/S Provisional) Shim, EF, 14mm; 42-5279-007-00 All Lots Persona TASP (Tibial A/S Provisional) Shim, GH, 10mm; 42-5279-007-01 All Lots Persona TASP (Tibial A/S Provisional) Shim, GH, 11mm; 42-5279-007-02 All Lots Persona TASP (Tibial A/S Provisional) Shim, GH, 12mm; 42-5279-007-03 All Lots Persona TASP (Tibial A/S Provisional) Shim, GH, 13mm; 42-5279-007-04 All Lots Persona TASP (Tibial A/S Provisional) Shim, GH, 14mm.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA Nationwide including DC, and PR and the countries of Australia, Austria, Belgium, Canada, Czech Republic, Dominican Republic, France, Germany, India, Iran, Israel, Italy, Japan, Luxembourg, Netherlands, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, United Arab Emirates, and United Kingdom.
  • Description du dispositif
    Persona (TASP) Tibial Articular Surface Provisional Shim, all sizes and Lots Catalog Number: 42-5279-002-00 thru 42-5279-009-04. || Product Usage: The Persona TASPs are sterilizable instruments Intended for multiple uses. The TASP components are used to aid the surgeon in assessing the thickness of the articular surface required. The TASP construct is utilized while conducting a trial range of motion. The TASP consists of 3 parts: a TASP bottom, a TASP shim, and a TASP top. The shims come in varying thicknesses to allow trialing for specific Articular Surface implant thicknesses.
  • Manufacturer
    Zimmer, Inc.
  • 1 Event
    • Rappel de Device Recall PERSONA
Device Recall TiBond
  • Modèle / numéro de série
    All revisions
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 || This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.
  • Manufacturer
    Spinal Elements, Inc
  • 1 Event
    • Rappel de Device Recall TiBond
Device Recall Conformis iTotal CR G2 Knee Replacement System
  • Modèle / numéro de série
    Serial Number: 0340552
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Distributed to IN.
  • Description du dispositif
    Conformis iTotal CR G2 Knee Replacement System || Catalog/Model #: M57250600010 || Intended for use as a total knee replacement in patients with knee joint pain and disability.
  • Manufacturer
    ConforMIS, Inc.
  • 1 Event
    • Rappel de Device Recall Conformis iTotal CR G2 Knee Replacement System
Device Recall The HemiCAP Contoured Articular Prosthetic
  • Modèle / numéro de série
    Catalog Number: 6105-0028, Part Number 1105-0028
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
  • Description du dispositif
    Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component; Catalog Number: 6105-0028, Pat Number 1105-0028. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
  • Manufacturer
    Arthrosurface, Inc.
  • 1 Event
    • Rappel de Device Recall The HemiCAP Contoured Articular Prosthetic
Device Recall The HemiCAP Contoured Articular Prosthetic
  • Modèle / numéro de série
    Catalog Number: 6125-0035, Part Number: 1125-0035
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
  • Description du dispositif
    Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component; Catalog Number: 6125-0035, Part Number: 1125-0035. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
  • Manufacturer
    Arthrosurface, Inc.
  • 1 Event
    • Rappel de Device Recall The HemiCAP Contoured Articular Prosthetic
Device Recall The HemiCAP Contoured Articular Prosthetic
  • Modèle / numéro de série
    Catalog Number: 8135-0032, Part Number: 3135-0032
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - USA nationwide. Internationally distributed to Europe, Canada, and Australia. Only products in US affected by this recall.
  • Description du dispositif
    Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component; Catalog Number: 8135-0032, Part Number: 3135-0032. HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing. Orthopedic shoulder prosthesis component.
  • Manufacturer
    Arthrosurface, Inc.
  • 1 Event
    • Rappel de Device Recall The HemiCAP Contoured Articular Prosthetic
  • 1
  • 2
  • 3
  • …
  • Next ›
  • Last »

À propos de cette base de données

Explorez plus de 120,000 rappels, alertes et avis de sécurité concernant les dispositifs médicaux, ainsi que leurs liens avec leurs fabricants.

  • FAQ
  • À propos de cette base de données
  • Contactez-nous
  • Crédits

Recevoir les newsletters de l'ICIJ

Vous travaillez dans le secteur médical? Vous avez vécu une expérience avec un dispositif médical? Notre projet n'est pas terminé. Nous souhaitons vous entendre.

Racontez-nous votre histoire !

Avertissement

Les dispositifs médicaux contribuent à diagnostiquer, prévenir et traiter de nombreuses blessures et maladies. Nous ne suggérons ou n'insinuons pas que des sociétés ou autres entités incluses dans la base de données internationale sur les dispositifs médicaux se livrent à un comportement illégal ou agissent de manière inappropriée. Le même implant peut avoir des noms différents selon les pays. Cette base de données n'a pas pour vocation de fournir des conseils aux patients. Ceux-ci doivent consulter leur médecin afin de déterminer si elle contient des informations pertinentes et si ces informations ont des implications médicales pour eux.

Téléchargez les données

La base de données internationale sur les dispositifs médicaux est sous licence Open Database License et ses contenus sous licence Creative Commons Attribution-ShareAlike. Toujours citer le Consortium international des journalistes d'investigation lorsque ces données sont utilisées. Vous pouvez télécharger une copie de la base de données ici.

Télécharger (zip)