Events

Rappel de Device Recall Mobile wDR motorized portable diagnostic Xray systems.

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 Sedecal S.A..

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
    73428
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1084-2016
  • Date de mise en oeuvre de l'événement
    2016-01-18
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2018-02-07
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=144185
  • 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
    System, x-ray, mobile - Product Code IZL
  • Cause
    This is related to previous 806 notifications about uncommanded movements of a motorized mobile x-ray system. reason for recall: along with the previously noted encoder and gauges problems and corresponding fixes, we have observed that static electricity can also elicit the unwanted behavior.
  • Action
    Philips Medical Systems sent an URGENT - Field Safety Notice letter dated August 6, 2014 was sent to all consignees of record informing them of a potential safety issue on the SEDECAL mobile units manufactured from May 2013 on. The firm requests the direct acounts with affected units should take the following steps: 1) The unit is equipped with a safety switch in the drive handle. If the drive handle is released the unit will stop; 2) Do not try to correct unintended movement using the controls on the drive handle; 3) Instead, stop the system immediately by releasing the drive handle entirely; 4) Alternatively, the emergency button can be pressed; 5) Take special care when the system crosses metal strips or plates on the floor or enters an elevator, as these are situations where electrostatic discharge is likely to occur; and, 6) Should the customer feel uncertain regarding this action, he/she can contact Philips Healthcare. Philips is preparing a Field Action Kit to replace the existing arrestor strap by a new arrestor with higher resistivity. This will reduce the electromagnetic pulse to a level, which is safe to not disturb the electronics. A Philips Service Engineer will contact the direct accounts to distribute Field Action Kit. The firm states that should direct accounts need to communicate with Philips in regards to this recall that they reference FC0-71200138. If they need any further information or support concerning this issue, please contact their local Philips representative.

Device

Device Recall Mobile wDR motorized portable diagnostic Xray systems.
  • Modèle / numéro de série
    Serial Numbers: 485886/SN11000007, 485062/SN11000009, 488169/SN11000011, 485061/SN11000012, 485059/SN11000013, 485060/SN11000015, 489089/SN11000016, 489616/SN11000033, 490027/SN11000034, 489694/SN11000035, 489695/SN11000036, 489696/SN11000037, 490221/SN11000039, 489088/SN11000040, 493566/SN11000047, 493565/SN11000048, 494867/SN11000051, 494941/SN11000052, 492417/SN11000053, 494456/SN11000055, 494865/SN11000056, 494864/SN11000060, 495286/SN11000061, 494866/SN11000062, 494464/SN11000065, 497570/SN11000066, 488171/SN11000068, 494060/SN11000070, 494061/SN11000071, 494062/SN11000072, 494063/SN11000073, 494064/SN11000074, 494065/SN11000075, 497715/SN11000080, 496446/SN11000082, 496387/SN12000003, 495938/SN12000007, 495939/SN12000008, 493364/SN12000022, 493462/SN12000023, 501028/SN12000026, 500739/SN12000027, 500740/SN12000028, 502424/SN12000034, 503143/SN12000036, 503142/SN12000037, 503141/SN12000038, 503144/SN12000039, 503541/SN12000040, 500466/SN12000045, 502721/SN12000047, 505077/SN12000048, 506626/SN12000051, 507607/SN12000054, 507906/SN12000055, 508342/SN12000057, 500468/SN12000058, 496401/SN12000059, 500467/SN12000060, 508838/SN12000061, 508532/SN12000062, 504450/SN12000064, 509718/SN12000068, 510607/SN12000072, 512160/SN12000077, 513477/SN12000080, 513478/SN12000081, 512892/SN12000082, 513848/SN12000084, 512887/SN12000085, 512888/SN12000086, 512890/SN12000087, 508699/SN12000088, 514462/SN12000089, 514461/SN12000090, 514104/SN12000091, 514103/SN12000092, 509062/SN12000107, 508783/SN12000108, 516891/SN12000110, 516896/SN12000111, 497572/SN12000112, 518135/SN12000118, 518342/SN12000119, 518343/SN12000120, 518344/SN12000121, 518345/SN12000122, 518346/SN12000123, 502025/SN12000124, 502026/SN12000125, 12000166, 519326/SN13000005, 519388/SN13000006, 519511/SN13000010, 519506/SN13000011, 519387/SN13000012, 519763/SN13000013, 519434/SN13000014, 520251/SN13000016, 520253/SN13000017, 519762/SN13000018, 520254/SN13000019, 520255/SN13000020, 520256/SN13000021, 520413/SN13000023, 520414/SN13000025, 520415/SN13000026, 520252/SN13000027, 520422/SN13000028, 520418/SN13000030, 520416/SN13000031, 520417/SN13000033, 522633/SN13000035, 522944/SN13000037, 523279/SN13000042, 523349/SN13000043, 13000046, 13000047, 13000048, 13000049, 13000053, 13000054, 13000055, 13000056, 13000057, 13000058, SN13000059, 13000060, SN13000061, SN13000062, SN13000063, 13000067, SN13000069, 13000070, 13000071, SN13000072, SN13000073, SN13000074, 13000075, 13000076, 13000077, 13000078, 13000079, SN13000080, SN13000082, SN13000083, SN13000084, 13000085, SN13000087, SN13000089, SN13000090, SN13000091, 13000092, 13000093, 13000094, SN13000099, SN13000100, SN13000101, SN13000102, SN13000103, SN13000104, SN13000106, SN13000107, 13000109, SN13000112, SN13000113, 519598/SN13000118, 519599/SN13000119, 519600/SN13000120, SN13000125, 13000127, 13000139, 13000140, 13000141, 13000143, 13000144, 13000145, SN13000146, SN13000147, SN13000148, SN13000149, SN13000153, SN13000154, SN13000157, SN7369686, SN13000159, SN13000160, SN13000163, SN13000164, SN13000165, 13000167, 13000168, 13000169, SN13000170, SN13000174, SN13000176, SN13000177, SN13000179, SN13000180, SN13000181, SN13000182, SN13000183, SN13000185, 13000196, 13000199, 13000200, 13000201, 13000202, 13000203, 13000204, 13000205, SN13000206, 14000004, 14000005, 14000006, 14000008, 14000009, 14000010, 14000011, 14000013, 14000014, 14000015, 14000016, 14000017, 14000019, 14000022, 14000024, 14000026, 14000028, 14000029, 14000031, 14000032, 14000033, 14000034, 14000037, 14000038, 14000041, 14000043, 14000046, 14000047, 14000048, 14000049, 14000050, 14000051, 14000052, SN14000061, 14000069, SN14000072, 14000075, 14000077, 14000078, 14000079, 14000080, 14000081, 14000082, 14000084, 14000086, 14000087, 14000088, 14000089, SN14000096, SN14000097, SN14000098, SN14000099, SN14000100, 14000092, 14000083, 14000085, 14000103, 14000106, 14000083, 14000109, 14000112, 14000116, 14000119, 14000118, 14000120, 14000121, 14000122, 14000124, SN14000128, 14000127, 14000126, SN14000130, 14000134, 14000135, 14000138, 14000139, SN15000002, 14100044, 14100045, 14100053, 14100054, 14100085, 14100086, 14100087, 14100088, 14100090, 14100094, 14100095, 14100097, 14100101, 14100104, 14100105, 14100109, 14100111, 14100117, 14100126, 14100127, 14100128, SN14100046, 15100019, 15100023, SN14100047, SN14100055, SN14100071, SN14100072, SN14100073, SN14100074, SN14100075, 15100028, 15100034, 15100035, 15100036, 15100039, 15100040, 15100041, 15100042, 15100047, 15100048, 15100050, 15100071, 15100084, 15100087, 15100088, 15100089, 15100091, 15100092, 15100093, 15100094, 15100095, 15100097, 15100098, 15100101, 15100103, 15100104, SN15100020, SN15100009, SN15100016, SN15100010, SN15100011, SN15100013 and SN15100018.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NM, NY, OH, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI.
  • Description du dispositif
    Mobile wDR motorized portable diagnostic X-ray systems. || Intended for use by a qualified/trained doctor or technologist on both adult and pediatric patients for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts on both adult and pediatric patients. Applications can be performed with patient sitting, standing or lying in the prone or supine positions. Not intended for mammography.
  • Manufacturer
    Sedecal S.A.

Manufacturer

Sedecal S.A.