Alerte Ou Avis De Sécurité sur All Pace Medical Inc temporary pacemakers and pacing system analysers (PSAs)

Selon Medicines and Healthcare products Regulatory Agency, ce/cet/cette alerte ou avis de sécurité concerne un dispositif en/au/aux/à United Kingdom qui a été fabriqué par Pace Medical Inc.

Qu'est-ce que c'est?

Les avis de sécurité sont des communications que les fabricants de dispositifs médicaux ou leurs représentants font parvenir en particulier aux travailleurs du secteur médical, mais aussi aux utilisateurs de ces dispositifs. Les avis de sécurité concernent les actions entreprises quant aux dispositifs présents sur le marché et peuvent inclure des rappels et des alertes.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert / Field Safety Notice
  • Numéro de l'événement
    MDA/2014/015
  • Date
    2014-05-14
  • Date de publication de l'événement
    2014-12-17
  • Pays de l'événement
  • Source de l'événement
    MHRA
  • URL de la source de l'événement
  • Notes / Alertes
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notes supplémentaires dans les données
    These devices are currently not on the EU market. Their CE-marking has been suspended because of quality system failings.In April 2014, Pace Medical’s subcontractor Devices Ltd, was audited by its notified body, BSI, with MHRA present as the observer. The audit found significant quality system failings relating to processes for complaint handling, post-market surveillance and vigilance, which included failures to implement corrective actions agreed at previous audits. As a result of this, on 9 April, the notified body suspended the EC-certification covering all devices manufactured by Pace Medical, except the pacing cables. Servicing of devices already in the field is unaffected by the suspension of the EC certificate.We are aware that UK hospitals use a range of temporary pacing cables and heart wires with temporary pacemakers. However, Pace Medical only holds validation data to confirm compatibility of their own cables with their pacemakers. Hospitals should continue to make a risk-based decision on the use of alternative, reusable or disposable cables or heart wires, based on availability and clinical need.The manufacturer is working with its notified body to prepare a corrective action plan to address the identified issues. The notified body will need to complete follow-up audits of Pace Medical’s actions before the EC-certification can be restored. If the situation changes, MHRA will issue further information.
  • Cause
    (pace medical inc) ce-marking suspended due to quality system failings. (mda/2014/015).
  • Action
    Be aware that as of 9 April 2014 this manufacturer is not able to sell these devices. However:any remaining Pace Medical devices purchased by distributors before this date can still be sold to UK hospitals servicing of Pace Medical devices can continue as before.Be aware that Pace Medical reusable temporary pacing cables, which have been validated by the manufacturer for compatibility with their temporary pacemakers, remain available for purchase.Be aware that the compatibility of alternative disposable or reusable cables with these pacemakers has not yet been fully validated by the manufacturer.Consult with the manufacturer or relevant distributors for further information on cable availability, where necessary.Consider the implications this has for the future provision of new devices within your hospital.

Device

  • Modèle / numéro de série
  • Description du dispositif
    All temporary pacemakers and pacing system analysers (PSAs) manufactured by Pace Medical Inc.
  • Manufacturer

Manufacturer

  • Adresse du fabricant
    Manufacturer’s authorised representativeSteven Hanson or Catherine Rose Devices Ltd 28 Fiddlebridge Industrial Centre Lemsford Road Hatfield Hertfordshire AL10 0DE Tel:    01707 327 641 Fax:  01707 266 677Email:  pacemedicalpres@gmail.com
  • Société-mère du fabricant (2017)
  • Source
    MHRA