Events

Retiro De Equipo (Recall) de Device Recall Belly Bag Urine Collection Bag with Hip Belt.

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Teleflex Medical.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    64715
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1158-2013
  • Fecha de inicio del evento
    2013-03-28
  • Fecha de publicación del evento
    2013-04-22
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2014-05-01
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=116842
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    Collector, urine, (and accessories) for indwelling catheter - Product Code KNX
  • Causa
    Sterile packaging may be compromised.
  • Acción
    Teleflex Medical sent an Urgent Medical Device Recall Notification dated March 28, 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Customers were instructed if you have any of the affected stock, immediately discontinue use and quarantine any products with the catalog numbers listed. If you and your customers have no affected stock please complete the enclosed Recall Acknowledgement Form and fax it to 1 (866) 804-9881 Attn: Customer Service. This will allow us to document your receipt of this letter. To return product complete the enclosed Recall Acknowledgement Form and fax it to 1 (866) 804-9881 Attn: Customer Service. This will allow us to document the amount of product you have on hand for return. If you have any other questions feel free to contact your local sales representative or Customer Service at 1 (866) 246-6990.

Device

Device Recall Belly Bag Urine Collection Bag with Hip Belt.
  • Modelo / Serial
    CATALOG NO. B1000 - 02A1100488, 02A1100489, 02A1100490, 02A1100491, 02A1100492, 02A1101420, 02A1101421, 02A1102009, 02A1102010, 02A1102049, 02A1102050, 02A1103180, 02A1103181, 02A1103182, 02A1201862, 02A1201868, 02A1201869, 02A1201870, 02A1201871, 02A1202372, 02A1202373, 02A1202374, 02A1202376, 02A1202377, 02A1202378, 02A1202603, 02A1202632, 02A1202633, 02A1202634, 02A1202783, 02A1202784, 02A1202785, 02A1202786, 02A1202787, 02A1202788, 02A1202789, 02A1202790, 02A1202791, 02A1202792, 02A1203552, 02A1203553, 02A1203554, 02A1203555, 02A1203556, 02A1204179, 02B1100522, 02B1100523, 02B1100524, 02B1101000, 02B1101001, 02B1101002, 02B1102328, 02B1102329, 02B1103007, 02B1200105, 02B1200106, 02B1200107, 02B1201685, 02B1201686 02B1201687, 02B1201688, 02B1201689, 02B1202029, 02B1202508, 02B1202509, 02C1000808, 02C1000910, 02C1000911, 02C1000912, 02C1001699, 02C1001725, 02C1002642, 02C1002655, 02C1002656, 02C1002657, 02C1002990, 02C1003816, 02C1003817, 02C1003818, 02C1100328, 02C1100329, 02C1100330, 02C1100331, 02C1103877, 02D1000274, 02D1000982, 02D1000983, 02D1002061, 02D1002062, 02D1002063, 02D1002753, 02D1002754, 02D1002755, 02D1200734, 02D1200735, 02D1200736, 02D1200737, 02D1203071, 02D1203072,  02D1203073, 02D1203074, 02D1203075, 02D1203084, 02E1002077, 02E1002746, 02E1002747, 02E1102105, 02E1102106, 02E1102107, 02E1102346, 02E1102347, 02E1102348, 02E1102349, 02E1102350, 02E1103220, 02E1103221, 02E1103222, 02E1103223, 02E1103225, 02E1200137, 02E1200138, 02E1200139, 02E1200140, 02E1200141, 02E1200142, 02E1200143, 02E1200144, 02E1201212, 02E1201234, 02E1201235, 02E1201236, 02E1201237, 02E1201238, 02E1201811, 02E1201812, 02E1201813, 02E1201983, 02E1201984, 02E1201985, 02E1201986, 02E1201987, 02E1201988, 02E1201989, 02F1000379, 02F1000380, 02F1001044, 02F1001045, 02F1001046, 02F1001801, 02F1001802, 02F1002742, 02F1002743, 02F1002744, 02F1003780, 02F1003781, 02F1003782, 02F1101266, 02F1102102, 02F1102107, 02F1102108, 02F1103126, 02F1103127, 02F1103128, 02F1103129, 02F1103566, 02F1103567, 02F1103568, 02F1103569, 02F1201733, 02F1202628, 02F1203156, 02F1203157, 02G1000133, 02G1000134, 02G1001110, 02G1001111, 02G1001112, 02G1001113, 02G1001114, 02G1001571, 02G1001572, 02G1002676, 02G1002677, 02G1002678, 02G1100575, 02G1100576, 02G1100577, 02G1100578, 02G1100579, 02G1200760, 02G1200771, 02G1200772, 02G1200773, 02G1200774, 02G1200775, 02G1201730, 02G1201731, 02G1201732, 02G1201733, 02G1201734, 02G1201736, 02G1202202, 02G1202203, 02G1202204, 02G1202205, 02G1202206, 02G1202207, 02G1202821, 02G1202822, 02G1202823, 02G1202824, 02G1202825, 02G1202826, 02H1000671, 02H1000672, 02H1000673, 02H1000674, 02H1000720, 02H1000721, 02H1000722, 02H1000723, 02H1001458, 02H1001459, 02H1001460, 02H1002831, 02H1002832, 02H1002833, 02H1100924, 02H1100925, 02H1100926, 02H1101672, 02H1101673, 02H1101674, 02H1101675, 02H1101676, 02H1102339, 02H1102340, 02H1102625, 02H1102626, 02H1102627, 02H1200264, 02H1200265, 02H1200267, 02H1200272, 02H1200275, 02H1201461, 02H1201462, 02H1201463, 02H1201464, 02H1201465, 02H1201466, 02H1201803, 02H1201804, 02H1201805, 02H1201806, 02H1201807, 02H1201809, 02H1202365, 02H1202367, 02H1203113, 02H1203114, 02H1203115, 02J1000130, 02J1000131, 02J1000132, 02J1000133, 02J1001054, 02J1001055, 02J1001056, 02J1001459, 02J1001460, 02J1001461, 02J1001662, 02J1001792, 02J1001793, 02J1002994, 02J1002995, 02J1003183, 02J1003184, 02J1003947, 02J1003948, 02J1101101, 02J1101102, 02J1101103, 02J1101104, 02J1101105, 02J1101766, 02J1101767, 02J1101768, 02J1101769, 02J1102135, 02J1102519, 02J1102520, 02J1102521, 02J1102524, 02J1103393, 02J1103394, 02J1103395, 02J1103396, 02J1103397, 02J1201479, 02J1201481, 02K1000440, 02K1000441, 02K1001417, 02K1001418, 02K1002226, 02K1002227, 02K1002623, 02K1003132, 02K1003133, 02K1003134, 02K1003595, 02K1100719, 02K1100720, 02K1100721, 02K1100722, 02K1100723, 02K1101650, 02K1101651, 02L1000684, 02L1000685, 02L1000686, 02L1000687, 02L1000688, 02L1001189, 02L1001190, 02L1002404, 02L1002405, 02L1002406, 02L1003281.02L1003282, 02M1000051, 02M1000060, 02M1001023, 02M1001024, 02M1001025, 02M1001026, 02M1001573, 02M1001574, 02M1001575, 02M1002665, 02M1002666, 02M1002667, 02M1002668, 02M1002669, 02M1003205, 02M1003206, 02M1003207, 02M1102661, 02M1102662   CATALOG NO. B1000P - 02A1100494, 02A1101101, 02A1102052, 02A1103184, 02A1201872, 02A1202793, 02B1101418, 02B1103009, 02B1202770, 02C1001701, 02C1002644, 02C1002993, 02C1201165, 02C1201848, 02C1202407, 02C1203284, 02D1002064, 02D1002756,  02E1200414, 02F1001047, 02F1001803, 02F1002745, 02F1100453, 02F1100454, 02F1203169, 02G1201452,  02G1202827, 02H1000675, 02H1001461, 02H1002834,  02H1102629, 02J1000134, 02J1003949, 02J1102523, 02K1002158, 02K1002624, 02K1101653, 02L1001192,  02L1002407, 02L1003284, 02L1101573, 02L1101575, 02M1000052, 02M1001027, 02M1001577, 02M1002671, 02M1003210,   CATALOG NO. B1000CT - 02A1100493, 02A1101100, 02A1102051, 02A1103183, 02B1101417, 02B1103008, 02E1201810, 02E1202328, 02E1202889, 02F1100452, 02G1101973, 02G1200493, 02G1200494, 02G1200495, 02G1201735, 02G1202208, 02G1202828, 02H1100292,  02H1102628, 02J1001061, 02J1001463, 02K1000442, 02K1001419, 02K1002228, 02L1001191, 02M1001576, 02M1002670, 02M1003209
  • Clasificación del producto
    Gastroenterology-Urology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA and the countries of Singapore, Canada, New Zealand, Germany, Ireland, Japan and Australia.
  • Descripción del producto
    Belly Bag Urine Collection Bag with Hip Belt. || The product is a sterile urine collection device that collects urine by mechanical means when attached to an indwelling Foley or suprapubic catheter.
  • Manufacturer
    Teleflex Medical

Manufacturer

Teleflex Medical
  • Dirección del fabricante
    Teleflex Medical, 4024 Stirrup Creek Dr, Durham NC 27703-9000
  • Empresa matriz del fabricante (2017)
    Teleflex Incorporated
  • Source
    USFDA