Events

Rappel de Device Recall Customed

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 Customed, 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
    68536
  • Classe de risque de l'événement
    Class 1
  • Numéro de l'événement
    Z-2504-2014
  • Date de mise en oeuvre de l'événement
    2014-05-20
  • Date de publication de l'événement
    2014-08-29
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2017-08-14
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=129537
  • 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
    Neurological tray - Product Code OJG
  • Cause
    Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). this could result in an injury to the patient due to product contamination or loss of sterility condition.
  • Action
    Customed Inc. sent a Recall Notification letter dated June 3, 2014 via email and followed by letter to all affected customers. The letter identified the affected products, problem and actions to be taken. The letter informed customers if the affected products are in their inventory to: 1. Remove products from sale (quarantine them) and cease distribution. 2. Complete and return the enclosed acknowledgement form to Customed Inc .Recall Coordinator. Affected products should be returned to Customed Inc for credit. Customers with questions were instructed to contact Customed Inc. Recall Coordinator at 1-787-801-0100 Ext. 7540

Device

Device Recall Customed
  • Modèle / numéro de série
    Code 900-2765, 6 lots 112124939 113036441 113056798 113057644 113078320 113088806
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.
  • Description du dispositif
    NEURO SPINE PACK || , CODE 900-2765 || CONTENTS: || (l ) DRAPE INCISION 23" X 1 7" || (I) SCALPEL W/HANDLE # 15 S/STEEL || (I) INSTRUMENT POUCH 7 X 1 1 2 COMPART || (I) Pk. STRIP SURGICAL W' X 6" || (I) CAUTERY PENCIL HAND SWITCHING LIF || (4) UTILITY DRAPE W/TAPE L/F || (I) SCALPEL W/HANDLE # 10 S/STEEL || (I) TUBE SUCTION CONNECT W' X I 2' LIF || (I) SKIN MARKER W/RULER || (2) SPECIMEN CONTAINER4oz W/LID & LABEL || (I) SOLUTION SURGICAL DURAPREP 26ML LIF || (I) YANKAUER SUCTION TUBE W/0 VENT LIF || (I) MAYO TRAY LARGE || (2) NEEDLE & BLADE COUNTER lOc MAG/CLEAR || (I) DRAPE INCISE ANTIMICROBIAL 23" X 1 7" LIF || (2) SYRINGE I Occ W/0 NEEDLE LUER LOCK LIF || (I) J VAC RESERVOIR 300ML || (2) LITE GLOVE LIF || (2) CAUTERY TIP POLISHER LIF || (2) TABLE COVER BTC 77" X 110" HD FULL L/F || (20) GAUZE SPONGE 4" X 4" 16PLY XRD LIF || (4) TOWELS ABSORBENT 1 5" X 20" LIF || ( I ) DRAPE T LAPAROTOMY 102" X 78" X 1 21" STD SMS (5) LAP SPONGE PREWASH 18" X 18" XRD LIF || ( I) SUTURE BAG FLORAL || (5) DRAPE 'l'4 ECONOMY 53" X 77" LIF || (3) GOWN IMPERVIOUS EXTRA REI NF. LGE T/WRAP || (I) UTILITY BOWL 1 6oz LIF || Product Usage: || EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
  • Manufacturer
    Customed, Inc

Manufacturer

Customed, Inc
  • Adresse du fabricant
    Customed, Inc, Calle Igualdad Final #7, Fajardo PR 00738
  • Société-mère du fabricant (2017)
    Customed Inc
  • Source
    USFDA