Events

Alerta De Seguridad para Trade name: Infusion Pump. Technical Name: Infusion Pump. ANVISA registration number: 80113010024. Risk class: III. Model Affected: N / A. 135002842; 135002843; 135002844; 135002845; 135002846; 135002847; 135002848; 135002849; 135002850; 135002851; 135002852; 135002853; 135002854; 135002855; 135002856; 135002857; 135002858; 135002859; 135002860; 135002861; 135002862; 135002863; 135002864; 135002865; 135002866; 135002867; 135002868; 135002869; 135002870; 135002871; 135002872; 135002873; 135002874; 135002875; 135002876; 135002877; 135002878; 135002879; 135002880; 135002881; 135002882; 135002883; 135002884; 135002885; 135002886; 135002887; 135002888; 135002889; 135002890; 135002891; 135026271; 135029940; 135044964; 135044977; 135044984; 135044987; 135044988; 135044989; 135044990; 135044991; 135044994; 135044996; 135044997; 135044998; 135044999; 135045018; 135045021; 135045027; 135045031; 135045035; 135045867; 135045873; 135045877; 135045881; 135045883; 135045884; 135045885; 135048038; 135048039; 135048040; 135048041; 135048042; 135048043; 135048045; 135048047; 135048048; 135048053; 135048054; 135048055; 135048057; 135048058; 135048059; 135048060; 135048061; 135048062; 135048064; 135048067; 135048069; 135048071; 135067003; 135067004; 135067005; 135067006; 135067008; 135067010; 135067012; 135067013; 135067014; 135067015; 135067017; 135067019; 135067021; 135067023; 135067024; 135101756; 135101757; 135101758; 135101759; 135101760; 135101761; 135101762; 135101763; 135101764; 135101765; 135101766; 135101767; 135101768; 135101769; 135101770; 135101771; 135101772; 135101773; 135101774; 135101775; 135101776; 135101777; 135101778; 135101779; 135101780; 135177845; 135180716; 135180717; 135180718; 135180719; 135180720; 135180721; 135180722; 135180723; 135180724; 135180725; 135180726; 135180727; 135180728; 135180729; 135180730; 135180731; 135180732; 135180733; 135180734; 135180735; 135180736; 135180737; 135180738; 135180739; 135180740; 135180741; 135180742; 135180743; 135180744; 135180745; 135180746; 135180747; 135180748; 135180749; 135180750; 135180751; 135180752; 135180753; 135180754; 135180755; 135180852; 135180853; 135180856; 135180857; 135180858; 135180859; 135180860; 135180861; 135180862; 135180863; 135180864; 135180865; 135180866; 135180867; 135180868; 135180869; 135180872; 135180873; 135180874; 135180875; 135180876; 135180877; 135180878; 135180879; 135180880; 135290455; 135309499; 135309500; 135309501; 135309502; 135309503; 135309504; 135309505; 135309506; 135309507; 135309508; 135309509; 135309510; 135309511; 135309512; 135309513; 135309514; 135309515; 135309516; 135309517; 135309518; 135309519; 135309520; 135309521; 135309522; 135309523; 135309524; 135309525; 135309526; 135309527; 135309528; 135309529; 135309530; 135309531; 135309532; 135309533; 135309535; 135309536; 135309537; 135309538; 135309539; 135309540; 135309541; 135309542; 135309543; 135309544; 135309545; 135309546; 135309547; 135309548; 135335853; 135335854; 135335855; 135335856; 135335857; 135335858; 135335859; 135335860; 135335861; 135335862; 135335863; 135335864; 135335865; 135335866; 135335867; 135335868; 800223130; 800223141; 800230698; 800246367; 800246486; 800246492; 800246494; 800246495; 800246503; 800246504; 800246513; 800246519; 800246520; 800253306; 800253452; 800253706; 800253708; 800253709; 800253756; 800253758; 800253770; 800253773; 800253790; 800253886; 800253887; 800253888; 800253890; 800253891; 800253893; 800253894; 800253897; 800253898; 800253899; 800254037; 800254038; 800264156; 800264407; 800265147; 800265148; 800265149; 800265150; 800265151; 800265152; 800265153; 800265154; 800265155; 800265156; 800265157; 800265159; 800265160; 800265163; 800265167; 800265169; 800265170; 800265172; 800265175; 800265177; 800265179; 800265180; 800265181; 800265182; 800265185; 800265187; 800265193; 800265202; 800265203; 800265208; 800265209; 800265210; 800265211; 800265215; 800265216; 800265217; 800265219; 800280535; 800280569; (...)

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por Respiratory Care Hospitalar Ltda; Carefusion 305 Uk Ltd/Bd Switzerland Sarl.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • ID del evento
    2375
  • Fecha
    2017-09-06
  • País del evento
    Brazil
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    Spring exchange. High priority should be given to clinical areas of neonates, pediatrics and critical care areas where critical drugs are administered at low infusion rates. If the plunger spring breaks, the pump will alarm "CHECK THE SYRINGE" and in this case be withdrawn from use until the spring is replaced. Spring replacement every 3 years of use of the pump as a preventive maintenance item. Special attention should be given to pumps for more than 3 (three) years from the date of manufacture. To identify the age of the pump, see the label on the back, where it is possible to check the date of manufacture. If you wish to notify technical complaints and adverse events use the following channels: Notivisa: Notices of adverse events (AE) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System. To access the System, you must register and select the Health Professional option, if you are a liberal professional or the Institution / Entity option, if you are a professional of an institution / entity. Technovigilance System: Patient or citizen can notify through the Technovigilance System / SISTEC access through the link Additional information: - Date of identification of the problem by the company: 08/30/2017 - Date of notification notice to Anvisa: 09/09/2017 The company that owns the affected product is responsible for contacting its customers in a timely manner. to ensure the effectiveness of the Field Action in progress. It stands out the joint responsibility of the distribution chain and use of health products in maintaining its quality, safety and efficacy, as well as the effectiveness of the Field Action, expressed by RDC 23/2012: "(...) Art 2 ° A holder of registration of health product is the holder of the registration / registration of health product with Anvisa. Single paragraph. The registration holder, as well as other agents involved from the production to the use of the product, or discarding it when applicable, are jointly and severally responsible for maintaining the quality, safety and efficacy of the health products to the final consumer. Art. 12 Distributors of health products shall forward to the registration holder, in a timely manner, the distribution map and other information requested for the notification and execution of field actions. (...) "
  • Causa
    Based on reports received from a customer in late 2016, bd / carefusion has identified a potential risk of syringe siphoning when used with alaris syringe pumps that have broken "plunger support spring". this spring is located located within the plunger support assembly.
  • Acción
    Field Action Code RA-2017-02-02 triggered under the responsibility of Respiratory Care Hospitalar Ltda. Field correction. Cont. batches affected: 800280605; 800280611; 800288773; 800289064; 800289121; 800289123; 800289124; 800289125; 800289128; 800289129; 800289130; 800289131; 800289133; 800289145; 800289155; 800289160; 800289165; 800289186; 800289226; 800289273; 800289274; 800289906; 800289963; 800289964; 800289974; 800289983; 800289986; 800290041; 800290185; 800290211; 800290238; 800290255; 800290258; 800290259; 800290261; 800290264; 800290267; 800290276; 800290278; 800290280; 800290281; 800290290; 800290293; 800290297; 800290298; 800290302; 800290309; 800290310; 800290313; 800290336; 800290338; 800290359; 800502728; 800504356; 800504358; 800504359; 800504363; 800504368; 800504378; 800504393; 800504399; 800504400; 800504404; 800504409; 800504414; 800506052; 800506152; 800506384; 800506393; 800506395; 800506396; 800506403; 800506406; 800506407; 800506409; 800506410; 800506411; 800506417; 800506418; 800506421; 800506426; 800506431; 800506433; 800506434; 800506435; 800506437; 800506441; 800506444; 800506448; 800506450; 800506453; 800506456; 800506457; 800506459; 800506461; 800506462; 800506463; 800506464; 800506467; 800506469; 800506471; 800506473; 800506474; 800506475; 800506476; 800506477; 800506480; 800506483; 800506484; 800506485; 800506488; 800506490; 800506491; 800506493; 800506494; 800506495; 800506497; 800506499; 800506500; 800506501; 800506502; 800506504; 800506505; 800506506; 800506508; 800511629; 135048046; 135048049; 135048066; 135048070; 135067000; 135067001; 135067002; 135067007; 135067009; 135067011; 135067016; 135067018; 135067020; 135067022; 800206637; 800208407; 800208478; 800208512; 800208532; 800208568; 800208591; 800208631; 800208644; 800208686; 800208736; 800214012; 800214015; 800214028; 800286101; 800510954; 800510957; 800510960; 800510973; 800510975

Device

Trade name: Infusion Pump. Technical Name: Infusion Pump. ANVISA registration number: 80113010024...

Manufacturer

Respiratory Care Hospitalar Ltda; Carefusion 305 Uk Ltd/Bd Switzerland Sarl
  • Source
    ANVSANVISA