Events

Rappel de Spacelabs Healthcare HookUp kits

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 Del Mar Reynolds Medical, 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
    60205
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0262-2012
  • Date de mise en oeuvre de l'événement
    2011-10-12
  • Date de publication de l'événement
    2011-11-21
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2012-02-23
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=104739
  • 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
    Degreaser, skin, surgical - Product Code KOY
  • Cause
    The non-sterile alcohol prep pads (b339) are included in spacelabs healthcare hook-up kits may have the presence of a bacterium, bacillus cereus. these alcohol prep pads were manufactured and recalled by professional disposables international (pdi).
  • Action
    SpaceLabs Healthcare sent an URGENT MEDICAL DEVICE CORRECTION letter dated October 21, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to immediately stop using the affected product and dispose of them per their hospital or clinic protocol. For questions contact Spacelabs Healthcare at 1-800-522-7025 and select 2 for Technical Support.

Device

Spacelabs Healthcare HookUp kits
  • Modèle / numéro de série
    B339 is listed on the PDI Alcohol Prep Pads.  Hook-up kits that contain the affected alcohol prep pads are as follows:  Aria, Kit Part number 23189-010, Kit, Basic hookup, AA; CardioCall, Kit Part number 23189-020, Kit, Hookup, CardioCall; Aria, Kit Part number 23189-106, Kit, Aria Hookup; Aria, Kit Part number 23189-110, Kit, Aria Hookup; Flashcorder, Kit Part number 23189-111, Kit, Flashcorder Hookup; Aria, Kit Part number 23189-113, Holter Hookup Kit 7 electrode; LifeCard 12, Kit Part number 23189-114, Kit, Hookup, LC12, Multilingual; Aria, Kit Part number 23189-115, Kit, Basic Hookup, AAA; LifeCard, Kit Part number 23189-116, Kit, Holter Hookup, LifeCard; 483, Kit Part number 23189-117, Kit, Holter Hookup 483; Aria, Kit Part number 23189-153, Holter Hookup Kit, 7 electrode; Aria VLC, Kit Part number 23189-207, Kit, Aria Hookup, VLC; EVO, Kit Part number 50-0048, 4 electrode hookup kit without pouch; EVO, Kit Part number 50-0049, 4 electrode hookup kit with pouch; EVO, Kit Part number SK10456, Sample Kit, Disposables.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - USA (natiowide) and the countries of South Africa, Turkey, Bangladesh, Dominican Republic, Peru, Belgium, Ecuador, Romania, Austria, Honduras, Guatemala, Denmark, Republic of Korea, Argentina, Thailand, Italy, Austria, Chile, Bolivia, Mexico, Sweden, Netherlands, Switzerland, India, Serbia, Australia, Morocco, Turkey, ISpain, Czech Republic, Slovakia, Poland, China, Columbia, Portugal, Canada, Germany, United Kingdom, Singapore, France, Russian Federation, Bahrain, and Kuwait
  • Description du dispositif
    PDI Electrode Prep Pads, Skin Prep B339 are non-sterile alcohol prep pads. They are included in the Spacelabs Healthcare Hook-Up kits. Each kit contains 2-4 pieces of PDI Electrode Prep Pads . || Hook-up kits that contain the affected alcohol prep pads are as follows: || Aria, Kit Part number 23189-010, Kit, Basic hookup, AA; || CardioCall, Kit Part number 23189-020, Kit, Hookup, CardioCall; || Aria, Kit Part number 23189-106, Kit, Aria Hookup; || Aria, Kit Part number 23189-110, Kit, Aria Hookup; || Flashcorder, Kit Part number 23189-111, Kit, Flashcorder Hookup; || Aria, Kit Part number 23189-113, Holter Hookup Kit 7 electrode; || LifeCard 12, Kit Part number 23189-114, Kit, Hookup, LC12, Multilingual; || Aria, Kit Part number 23189-115, Kit, Basic Hookup, AAA; || LifeCard, Kit Part number 23189-116, Kit, Holter Hookup, LifeCard; || 483, Kit Part number 23189-117, Kit, Holter Hookup 483; || Aria, Kit Part number 23189-153, Holter Hookup Kit, 7 electrode; || Aria VLC, Kit Part number 23189-207, Kit, Aria Hookup, VLC; || EVO, Kit Part number 50-0048, 4 electrode hookup kit without pouch; || EVO, Kit Part number 50-0049, 4 electrode hookup kit with pouch; || EVO, Kit Part number SK10456, Sample Kit, Disposables. || A surgical skin degreaser or an adhesive tape solvent is a device that consists of a liquid such as 1,1,2-trichloro-1,2,2-trifluoroethane; 1,1,1-trichloroethane; and 1,1,1-trichloroethane with mineral spirits intended to be used to dissolve surface skin oil or adhesive tape.
  • Manufacturer
    Del Mar Reynolds Medical, Ltd.

Manufacturer

Del Mar Reynolds Medical, Ltd.
  • Adresse du fabricant
    Del Mar Reynolds Medical, Ltd., 1-2 Harforde Ct., Foxholes, Business Park, Hertford United Kingdom
  • Société-mère du fabricant (2017)
    OSI Systems Inc
  • Source
    USFDA