Events

Rappel de Device Recall Tyvek SelfSeal Pouch with STERRAD Chemical Indicator

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 Advanced Sterilization Products.

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
    56367
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1393-2011
  • Date de mise en oeuvre de l'événement
    2010-06-23
  • Date de publication de l'événement
    2011-02-22
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2012-03-14
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=93317
  • 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
    Sterilization Wrap Containers, Trays, Cassettes & Other Accessories - Product Code KCT
  • Cause
    The recall was initiated after advanced sterilization products (asp) discovered a non-conforming lot. the misaligned perforations may have caused the seal to be incomplete on some of the pouches, creating a potential breach for pouches being used to store sterilized equipment on shelves.
  • Action
    Advanced Sterilization Products (ASP) released Urgent: Product Recall notifications to its consignees identifying the affected product and explaining the reason for recall. The letter also discussed the impact of using this affected product and return instructions. The firm asked customers to examine their inventory, discontinue use of Tyvek Self-Seal Pouch with STERRAD Chemical Indicator 12332 and to return all unused affected products to Stericycle. Customers are to complete the Business Reply Card and return it to Stericycle.

Device

Device Recall Tyvek SelfSeal Pouch with STERRAD Chemical Indicator
  • Modèle / numéro de série
    Lot Number: 2020
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- USA, Argentina, Australia, Canada, Chile, Czech Republic, Hong Kong, India, Japan, Panama, Peru and Puerto Rico.
  • Description du dispositif
    Tyvek Self-Seal Pouch with STERRAD Chemical Indicator 12332. || Intended to be used to contain medical devices that are being terminally sterilized in STERRAD Sterilization Systems.
  • Manufacturer
    Advanced Sterilization Products

Manufacturer

Advanced Sterilization Products
  • Adresse du fabricant
    Advanced Sterilization Products, 33 Technology Drive, Irvine CA 92618
  • Société-mère du fabricant (2017)
    Johnson & Johnson
  • Source
    USFDA