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-2352-2014
  • 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=129246
  • 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
    Angiography/angioplasty kit - Product Code OEQ
  • 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 900-796, 14 lots: 113047032 113057507 113067965 113078346 113088892 113109873 131110279 131210842 140111251 140211700 140311949 140312388 140513145 140513340
  • Classification du dispositif
    Cardiovascular 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
    FEMORAL ANGIOGRAPHY PACK - || (1) TABLE COVER REINFORCED 50" X 90" UF || (1) GOWN LARGE SMS IMPERVIOUS REINFORCED LIF || (1) TOWEL ABSORBENT 15" X 20" UF || (1) DRAPE ANGlO 75" X 145" || (4) TOWELS CLOTH HUCK (BLUE) UF || (3) SYRINGE 1 Occ WITHOUT NEEDLE LUER LOCK UF || (1) IV ADM SET 15ML 1 06" LONG LIF || (20) GAUZE SPONGE 4" X 4" 12PL Y LIF || (1) NEEDLE HYPODERMIC 18G X 1Y:. ST. UF || (1) NEEDLE HYPODERMIC 21G X 1Y:. ST. LIF || (2) MEDICINE CUP 2oz. CLEAR LIF || (1) SCALPEL WEIGHTED SAFETY #11 || (2) CHLORASCRUB SWABSTICK 5.1 ML LIF || (1) GOWN SURG REINFORCED LARGE TOWEL/WRAP LIF || (1) SPECIMEN CONTAINER 4oz. W/LID & LABEL LIF || (1) NEEDLE HYPODERMIC 25G X 5/8 ST. LIF || (1) SYRINGE 3cc WITHOUT NEEDLE LUER LOCK LIF || (1) FORCEP ADS ON TISS. WITH TIP LIF || (1) UTILITY BOWL 32oz LIF || (1) UTILITY BOWL 16oz L/F || (1) FORCEP KELLY STRAIGHT 5.5" LIF || (1) MOSQUITO HALSTED CVD 5" LIF || (1) TRAY ORGANIZER FULL DEEP LIF || (1) SCISSOR MAYO 6.75 STRAIGHT LIF || (1) HOLDER NEEDLE WEBSTER 4.75 LIF || (1) GUIDEWIRE .035" X 150cm UF || (1) TIME OUT BEACON NON WOVEN ST. UF || (1) MAYO TRAY SMALL LIF || (2) TOWEL CLAMP UF || (2) BAG BAND RUBBAND & TAPE LIF || (1) Pr. GLOVE SURG. #7Y:. DERMA PRENE P/F LIF || (2) SYRINGE 20cc WITHOUT NEEDLE LUER LOCK LIF || LABEL SAMPLE || (1) NEEDLE & BLADE COUNTER 60C FOAM STRIP/MAG STRIP LIF || (1) NEEDLE 18G X 2 o/.i AMC/4 || (1) SKIN MARKER INK WITH/8 LABEL || 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