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-2525-2014
  • 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=129567
  • 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
    900-3115, 2 lots: 131211011 140111439
  • 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
    Liposuction Pack FJG, code 900-3115, contains: || (2) GOWN LARGE SMS IMPERVIOUS REINFORCED AAMIIII LIF || (2) TOWEL ABSORBENT 15" X 20" LIF || (1) NEEDLE HYPODERMIC 25 X 1 LIF || (1) BOWL UTILITY QUART 32oz LIF || (1) COVER MAYO STAND REINFORCED L/F || (20) GAUZE SPONGE 4" X 4" 16PLY LIF || (1) COVER TABLE REINFORCED 44" X 78" LIF || (2) CUP DENTURE 8oz TEAL WITH LID LIF || (6) TOWEL CLOTH HUCK BLUE LIF || (1) SAFETY SCALPEL #15 DISPOSABLE LIF || (1) SYRINGE 10CC WITHOUT NEEDLE LUER LOCK LIF || (4) DRAPE UTILITY WITH TAPE L/F || (1) SHEET% DRAPE REINFORCED 60" X 77" LIF || (1) PR. GLOVE SURG. CUSTOMGUARD CHLOROPRENE #7 P/F L/F || (2) PR. GLOVE SURG CUSTOMGUARD CHLOROPRENE #6.5 P/F L/F || (1) DRAPE TOP WITH ADHESIVE 108" X 50" STD SMS L/F || (1) DRAPE BOTTOM ABS REINF. 71" X 62" STD SMS WITH TAPE L/F || (2) DRAPE SIDE 42" X 76" WITH TAPE LIF || (1) PVP IODOPHOR BOTTLE 4oz PAINT || (1) SUCTION TUBING 8' X 3/8" ID NON CONDUCTIVE LIF || (1) STRIP STERI CLOSURE Y2" X 4" || 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