Events

Rappel de Device Recall AMPLATZER Delivery Systems

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 AGA Medical Corporation.

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
    30481
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0356-05
  • Date de mise en oeuvre de l'événement
    2004-11-23
  • Date de publication de l'événement
    2004-12-24
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2006-12-26
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=36275
  • 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
    unknown device name - Product Code BGK
  • Cause
    Tubing utilized in the manufacture of the amplatzer delivery and exchange system sheaths and dilators was in some cases manufactured by our supplier outside of process parameters; causing a residue to be left on the inside of the tubing.
  • Action
    Recall notices were sent via e-mail 11/22/04 to physicians, hospitals and distributors who received affected product. Hard copies of the Recall Notices were sent to all customers (international and domestic) via Federal Express 11/22-24/04. A form that is attached to the Recall Notice asks for customers to fill out quantities of affected product and to return the affected product to AGA Medical.

Device

Device Recall AMPLATZER Delivery Systems
  • Modèle / numéro de série
    M01I13-3, M02E14-03, M02E16-24, M02E16-30, M02F05-20,  M02G10-04, M02G23-05, M02H19-01, M02H30-01, M02K07-03,  M02K12-07, M02L02-24, M02L02-27, M02L11-11, M02L19-08,  M03A09-16, M03A22-11, M03B10-53, M03F13-06, M03F19-13,  M03G10-37, M03H08-06, M03H15-07, M03J04-05, M03J17-05,  M03J25-26, M03K01-02, M03K09-22, M03K14-05, M03K16-16,  M03K16-17, M03K24-09, M03L18-56, M03M30-11, M03M30-14,  M03M30-15, M04A19-30, M04B03-11, M04B17-34, M04B24-09,  M04C30-08, M04F08-20, M04F23-20, M04F28-46, M04G01-19,  M04G01-21, M04H23-20, M04H23-21, M04J07-04
  • Distribution
    Product has been distributed throughout the US and Internationally, including Canada, Europe and Australia.
  • Description du dispositif
    AMPLATZER Delivery System 45-degree curve, order no. 9-DEL-10F-45/80. Product is labeled as Sterile EO. || Amplatzer Occluder Device and Delivery System is comprised of delivery sheath, delivery cable, dilator, loading device and pin vise. The Delivery and Exchange Systems are placed onto polyboard backing cards. The backing card is then placed into a smaller of 2 Tyvek pouches. The pouch is then placed inside a larger Tyvek pouch. The kit is assembled at AGA and then sterilized by Steris, Minneapolis, MN.
  • Manufacturer
    AGA Medical Corporation

Manufacturer

AGA Medical Corporation
  • Adresse du fabricant
    AGA Medical Corporation, 682 Mendelssohn Ave N, Golden Valley MN 55427-4306
  • Source
    USFDA