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-2419-2014
  • 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=129313
  • 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
    General surgery tray (kit) - Product Code LRO
  • 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
    Product code 900-1922, 21 lots: 110112626 112010102 112030659 112041213 112051899 112062468 112081922 113025826 113036785 113057439 113078286 113088772 113089202 113109767 131110213 140111080 140111186 140211803 140312097 140312460 140412890
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • 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
    AV FISTULA PACK- || (1) DRAPE T LAPAROT 102" X 78" X121 " STD SMS || (3) GOWN SURG. REINFORCED X-LARGE EXTRA LONG LEVEL IV || (1) DRAPE SHEET 42" X 57" SMS || (4) DRAPE UTILITY WITH TAPE LIF || (1 0) GAUZE SPONGE 4" X 4" 16PL Y XRD LIF || (1) PENCIL CAUTERY HAND SWITCHING LIF || (1) TUBE SUCTION CONNECT "Y-1" X 12' LIF || (1) FRAZIER WITH CONTROL VENT & OBTUR 10F LIF || (2) LITE GLOVE LIF || (1) BOWL UTILITY 32oz LIF || (2) BOWL UTILITY 16oz LIF || (10) LAP SPONGE PREWASH XRD LIF || (1) SOLUTION SURGICAL DURAPREP 26ML LIF || (3) SYRINGE 60ML WITHOUT NEEDLE LUER LOCK LIF || (1) SYRINGE 30CC WITHOUT NEEDLE LUER LOCK UF || (1) SYRINGE 5CC WITH NEEDLE 21G X 1% LUER LOCK UF || (2) SYRINGE 3CC WITHOUT NEEDLE LUER LOCK UF || (1) NEEDLE HYPODERMIC 18G X 1 % || (2) COUNTER NEEDLE & BLADE 10C MAG/CLEAR UF || (1) COVER MAYO STAND REINFORCED LIF || (1) COVER TABLE 44" X 90" || (1) MAYO TRAY SMALL || (2) ABSORBENT TOWEL 15" X 20" UF || (1) BOWL WITH LID PLASTIC 80oz || 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