Alerte De Sécurité sur INSTRUMENTS PFC AND SPECIALIST (Instrument Intramedullary Specialist 2 (SP 2 IM) 400mm (PN 96-6120)) - Registration No. 10132590285 - Lot: C4GA54, Lot: TBAGG, Lot: H0302, Lot: H0401, Lot: H0610, Lot : H0710, Lot: H0810, Lot: H1008, Lot: H0999

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda; DEPUY INTERNATIONAL LTD.

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • ID de l'événement
    1734
  • Date
    2015-11-13
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 data from the U.S. and Brazil.
  • Notes supplémentaires dans les données
    The company informs that if the affected 400mm (SP 96-6120) IM SP2 Rod Tool breaks during surgery and a portion of the rod stays in the patient, the possible clinical implications are: • If observed during surgery: - Significant delay in surgery due to the attempt to remove the remaining stem; - Minor bone damage due to attempted removal of the remaining rod. • If not observed during surgery: - An adverse reaction may occur because the fractured shaft, if not removed from inside the bone, can act as a stressor causing bone remodeling and inflammation; - Pain during possible bone remodeling or during Magnetic Resonance Imaging (MRI) exams. DePuy does not recommend a prophylactic review in the absence of symptoms. If a surgeon performed a procedure using an affected instrument and it broke, the company recommends that the surgeon discuss the potential clinical implications and risks with symptomatic patients. Sharing this information will allow surgeons to discuss the problem and provide follow-up recommendations.
  • Cause
    The company received complaints regarding affected batches, stating that the stem broke and a portion of the stem was left in the patient. all complaints involve the 400 mm im sp2 rod tool (pn 96-6120) made of 455 ss alloy. the company identified the failure potential of the 400 mm haste im sp2 instrument, manufactured with 455 ss alloy, due to fatigue and / or overloading by applying excessive leverage to the 400 mm shank im sp2 instrument (pn 96-6120).
  • Action
    DePuy directs that the affected batches of the 400mm Haste IM SP2 IM Instruments (PN 96-6120) be immediately discontinued. i) identify if they have any of the instruments involved in this field action and return the affected instruments immediately; ii) Kits containing 400mm Rods SP 400 Instruments (PN 96-6120) include: - SIGMA SP2 Primary Instrument Sets, - SIGMA HP Primary Instrument Sets, - PFC Sigma TC3 Revision Instrument Sets. Refer to the "Instrument Options" section of the Letter to the Customer (Appendix II) for alternatives to the 400mm Rod Tool IM SP2 (PN 96-6120). -16)