Rappel de U-100 Insulin Syringe 0.5mL 27G and 29G

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Terumo Australia Pty Ltd.

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
    RC-2018-RN-00171-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2018-02-23
  • Pays de l'événement
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
  • Notes / Alertes
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Notes supplémentaires dans les données
  • Cause
    Taechang industrial is initiating a recall of all lot numbers of terumo branded u-100 insulin syringe with a capacity of 0.5ml x 27g and 29g due to incorrect information contained on the device peel pack.The statement:"0.5ml single use syringe for 100 units or less in two unit increments"is incorrect and should state:"0.5ml single use syringe for 50 units or less in one unit increments"in essence, the 0.5ml peel packs have been inadvertently printed with information intended for the 1.0ml peel pack. the printing on the syringes themselves is correct.
  • Action
    Terumo is requesting customers: 1. Review the supplied urgent medical device recall (permanent removal) notification, inspect all stock on hand and quarantine affected lot numbers prior to return as per the instructions given in the customer letter. Ensure all relevant staff are made aware of this recall; 2.If any of the recalled product could have been transferred from your facility to another, please immediately notify that facility know of this recall; 3.Where possible, return all affected stock to your supply department for consolidated return to Terumo Australia as per the instructions given; and 4.Terumo will be providing credit for all returned stock. Replacement stock will not be automatically issued. Please process a new order if more stock is required.

Device

  • Modèle / numéro de série
    U-100 Insulin Syringe 0.5mL 27G and 29G Lot Numbers for product SS*05M2713KA: 7D700, 7E700, 7F731, 7G719, 7I701, 6H713,6K700 Lot Numbers for product SS*05M2913KA : 7A713, 7G720, 7I7012, 7A713, 7B728, 6F700, 6F706Multiple Lot Numbers (see attached)ARTG: 234082 (Terumo Australia Pty Ltd - Insulin syringe, fixed-needle)
  • Manufacturer

Manufacturer