Events

Rappel de Device Recall Trauma Large Screws

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Zimmer, Inc..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    68818
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2549-2014
  • Date de mise en oeuvre de l'événement
    2014-07-22
  • Date de publication de l'événement
    2014-08-26
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2015-09-15
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=129073
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    Screw, fixation, bone - Product Code HWC
  • Cause
    Zimmer is recalling sterile-packaged implants and instruments packaged in six different package configurations due to packaging design verification test failures. specifically, multiple test samples from each of the six configurations failed simulated distribution and shipping testing when the devices either breached inner or outer package trays or seal integrity was lost.
  • Action
    Zimmer sent an URGENT MEDICAL DEVICE RECALL letter dated July 2014 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. Please call the Customer Call Center at 1-800-348-2759 for questions or concerns involving this notice.

Device

Device Recall Trauma Large Screws
  • Modèle / numéro de série
    Item Numbers 00114610099, 00114610500, 00114610532, 00114610599, 00114611000, 00114611032, 00114611099, 00114611500, 00114611532, 00114611599, 00114612000, 00114612032, 00114612099, 00114612500, 00114612599, 00114613000, 00114613099, 00225210555, 00225211055, 00225211555, 00225212055, 00225212555, 00225213055, 00225710565, 00225711065, 47234712005, 47234712400, 47234712440, 47234712500, 47234712600, 47234810535, 47234811035, 47235910055, 47248310560, 47248311060, 47248311560, 47248312060, 47248312560, 47248313060, 47248313560, 47248314060, 47248410560, 47248411060, 47248411560, 47248412060, 47248412560, 47248413060, 47248413560, 47248414060, 47348310560, 47348311060, 47348311560, 47348312060, 47348312560, 47348313060, 47348313560, 47348314060, 47348410560, 47348411060, 47348411560, 47348412060, 47348412560, 47348413060, 47348413560, 47348414060, 47483510500, 47483510501, 47483511000, 47483511001, 47483511500, 47483511501, 47483512000, 47483512001, 47483512500, 47483513000, 47483513500, 47483514000, 47483514500, 47483515000, 47484510501, 47484511001, 47484512001, 47486510500, 47486510501, 47486510502, 47486511000, 47486511001, 47486511002, 47486511502, 47486512002 EXPIRATION DATE PRIOR TO 2024-07
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution.
  • Description du dispositif
    Trauma Large Screws: || CANN BONE SCREW 7.0MMX100MMLG || CANN BONE SCREW 7.0X105LG || CANN BONE SCREW 7.0X105LG || CANN BONE SCREW 7.0MMX105MMLG || CANN BONE SCREW 7.0X110LG || CANN BONE SCREW 7.0X110LG || CANN BONE SCREW 7.0MMX110MMLG || CANN BONE SCREW 7.0X115LG || CANN BONE SCREW 7.0X115LG || CANN BONE SCREW 7.0MMX115MMLG || CANN BONE SCREW 7.0X120LG || CANN BONE SCREW 7.0X120LG || CANN BONE SCREW 7.0MMX120MMLG || CANN BONE SCREW 7.0X125LG || CANN BONE SCREW 7.0MMX125MMLG || CANN BONE SCREW 7.0X130LG || CANN BONE SCREW 7.0MMX130MMLG || RECON SCR LGE 5.5MMDX105MM || RECON SCR LGE 5.5MMDX110MM || RECON SCR LGE 5.5MMDX115MM || RECON SCR LGE 5.5MMDX120MM || RECON SCR LGE 5.5MMDX125MM || RECON SCR LGE 5.5MMDX130MM || ITST ANTI-ROT SCR 6.5MMDX105MM || ITST ANTI-ROT SCR 6.5MMDX110MM || PERI. SCR 3.5MM X105MML || PERI SCR. 6.5MM X 100MM L || PERI SCR. 6.5MM X 140MM L || PERI SCR. 6.5MM X 100MM L || PERI SCR. 6.5MM X 100MM L || 3.5MM CORT SCR X 105MM SELFTAP || 3.5MM CORT SCR X 110MM SELFTAP || 5.5MM X 100MM CANN LKNG SCREW || Z NAIL 6.0 X 105 CANC SCREW PT || Z NAIL 6.0 X 110 CANC SCREW PT || Z NAIL 6.0 X 115 CANC SCREW PT || Z NAIL 6.0 X 120 CANC SCREW PT || Z NAIL 6.0 X 125 CANC SCREW PT || Z NAIL 6.0 X 130 CANC SCREW PT || Z NAIL 6.0 X 135 CANC SCREW PT || Z NAIL 6.0 X 140 CANC SCREW PT || Z NAIL 6.0 X 105 CANC SCREW FA || Z NAIL 6.0 X 110 CANC SCREW FA || Z NAIL 6.0 X 115 CANC SCREW FA || Z NAIL 6.0 X 120 CANC SCREW FA || Z NAIL 6.0 X 125 CANC SCREW FA || Z NAIL 6.0 X 130 CANC SCREW FA || Z NAIL 6.0 X 135 CANC SCREW FA || Z NAIL 6.0 X 140 CANC SCREW FA || Z NAIL 6.0 X 105 CANC SCREW PT || Z NAIL 6.0 X 110 CANC SCREW PT || Z NAIL 6.0 X 115 CANC SCREW PT || Z NAIL 6.0 X 120 CANC SCREW PT || Z NAIL 6.0 X 125 CANC SCREW PT || Z NAIL 6.0 X 130 CANC SCREW PT || Z NAIL 6.0 X 135 CANC SCREW PT || Z NAIL 6.0 X 140 CANC SCREW PT || Z NAIL 6.0 X 105 CANC SCREW FA || Z NAIL 6.0 X 110 CANC SCREW FA || Z NAIL 6.0 X 115CANC SCREW FA || Z NAIL 6.0 X 120CANC SCREW FA || Z NAIL 6.0 X 125 CANC SCREW FA || Z NAIL 6.0 X 130 CANC SCREW FA || Z NAIL 6.0 X 135 CANC SCREW FA || Z NAIL 6.0 X 140 CANC SCREW FA || 3.5X105 CORT SCR || 3.5 X 105 CORT SCR SELF TAP || 3.5X110 CORT SCR || 3.5 X 110 CORT SCR SELF TAP || 3.5X115 CORT SCR || 3.5 X 115 CORT SCR SELF TAP || 3.5X120 CORT SCR || 3.5 X 120 CORT SCR SELF TAP || 3.5X125 CORT SCR || 3.5X130 CORT SCR || 3.5X135 CORT SCR || 3.5X140 CORT SCR || 3.5X145 CORT SCR || 3.5X150 CORT SCR || 4.5 X 105 CORT SCR SELF TAP || 4.5 X 110 CORT SCR SELF TAP || 4.5 X 120 CORT SCR SELF TAP || 6.5X105 CANC SCR, FULLY THDED || 6.5X105 CANC SCR, 16MM THD || 6.5X105 CANC SCR, 32MM THD || 6.5X110 CANC SCR, FULLY THDED || 6.5X110 CANC SCR, 16MM THD || 6.5X110 CANC SCR, 32MM THD || 6.5X115 CANC SCR, 32MM THD || 6.5X120 CANC SCR, 32MM THD
  • Manufacturer
    Zimmer, Inc.

Manufacturer

Zimmer, Inc.
  • Adresse du fabricant
    Zimmer, Inc., 1800 W Center St, Warsaw IN 46580-2304
  • Société-mère du fabricant (2017)
    Zimmer Biomet Holdings
  • Commentaire du fabricant
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    USFDA