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-2309-2014
  • 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=129142
  • 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
    Obstetrical kit - Product Code OKV
  • 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 900-168, 34 lots: 110061523 110092042 110092166 110092388 110112612 110123053 111010060 111020331 111041058 111051332 111061506 111071775 111082059 111102842 111113023 111123371 112072440 112083401 112114642 112125025 113026049 113036454 113036752 113057838 113078270 113088750 113089158 113109744 131110336 140111166 140211649 140211925 140513102 140513461
  • Classification du dispositif
    Obstetrical and Gynecological 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
    Customed LABOR & DELIVERY PACK - Includes: || (1) TABLE COVER 44" x 90" || (2) LEGGINS WITH/7" CUFF 30" x 42" || (5) ABSORBENT TOWELS 15" x 20" LIF || (1) BABY BLANKET PRINTED LIF || (2) PAD OBSTETRICAL XLGE LIF || (1) EAR ULCER SYRINGE 2oz. LIF || (1) BABY BLANKET POLY ABS. IMP. LIF || (1) Pr. SURGICAL GLOVE # 7Y2 || (1) UNDER BUTTOCK DRAPE WITH POUCH || (1) BEANNIES BABY LIF || (1) FEEDING TUBE 8 Fr. 15" LONG LIF || (1) ABDOMINAL DRAPE WITH TAPE L/F || (1) DRAPE SHEET 41 " X 58" SMS || (1) GOWN SURG. REINFORCED X-LARGE SMS LEVEL IV || (1) VAGINAL SPONGE XRD || (1) UMBILICAL CORD CLAMP LIF || (2) CLOTH HUCK TOWELS BLUE || (1 0) GAUZE SPONGE 4" X 4"16 PLY XRD LIF || (1) SYRINGE 1 Occ WITH NEEDLE 21 X 1 Y2 || (1) MUCUSTRAP 20cc 1 OFr. || (1) BOWL PLASTIC 80oz WITH LID || (1) WRAPPER 24" X 24" LIF || 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