Events

Recall of Device Recall PrecisePLAN Treatment Planning System

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Elekta, Inc..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    57692
  • Event Risk Class
    Class 2
  • Event Number
    Z-1476-2011
  • Event Initiated Date
    2008-01-28
  • Event Date Posted
    2011-03-02
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2011-04-21
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=97012
  • Notes / Alerts
    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.
  • Extra notes in the data
    System, planning, radiation therapy treatment - Product Code MUJ
  • Reason
    Preciseplan generates digitally reconstructed radiographs (drr;s) with a shift in the superior direction.
  • Action
    Elekta sent an Important Notice A308 letter dated January 28, 2008, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to contact their Elekta representative directly if they had any questions. .

Device

Device Recall PrecisePLAN Treatment Planning System
  • Model / Serial
    0800690937B9, 080069079BB3, 0800690CED1C, 080069104499, 0800690E7F53, 0800690C1E5A, 0800690EAE97, 08006902EA0A, 08006902E9E0, 080069107C1F, 08006907BB8E, 08006907BB55, 08006902E7D1, 0800690C934D, 080069104115, 08006909FA29, 0800690978E3, 080069086F92, 0800690A02F6, 080069107C11, 0800690A8F4C, 0800690A90FD, 0800690E6CF9, 0800690CF7A2, 0800691003C3, 080069100455, 0800690ED7C0, 0800690ED7DF, 0800690EB787, 08006910762C, 080069098EF6, 0800690C1745, 0800690CE157, 080069108174, 0800690909B4, 0800690761D1, 08006909F50B, 0800690977ED, 08006909355C, 080069132DDF, 080069100706, 080069107262, 08006909D95A, 08006907CA22, 08006907999A, 0800691064DE, 0800690ED967, 0800691075FB, 0800690ABEC5, 0800690840A8, 080069087720, 080069076227, 08006908EC10, 08006902EB35, 08691003D7, 0800690A13FB, 0800690C208F, 0800690C228, 0800690E9B4E, 080069087740, 08006907CA1C, 08006905E180, 08006905E6BA, 0800690E8CA9, 080069E9AB7, 08006905C433, 08006907BEDF, 08006905BA2D, 0800690A8793, 0800690A02F5, 080069090841, 08006908F51D, 080069086630, 0800690907F5, 0800690907CD, 0800690A740E, 0800690A7410, 0800690AC55B, 0800690ACA88, 08009607D4EF, 08006907D6B8, 08006907BB82, 0800690A0FE2, 0800690A8E1F, 080069100F95, 0800690937B1, 08006908EDF3, 080069107CB2, 0800690E964F, 0800690EA07F, 0800690883CB, 0800691077E0, 08006910561E, 0800690EC1DD, 0800690E72DF, 08006907C7A1, 080069076BF4, 0800690C9B17, 0800690A0FF6, 0800690A0FEF, 0800690C9148, 0800690A2863, 0800690906AE, 08006907F138, 08006905E498, 0800690ED72E, 0800690ED90E, 0800690C90F4, 08006902E918, 0800690E9F8A, 08006905E723, 08006908ED1C, 080069105594, 0800690C0D48, 0800690AB49C, 0800690C9357, 0800690A02F3, 0800690A47CF. 0800690C54B2, 08006909F10F, 08006907BB89, 08006907BB7F, 08006907B074, 08006907B129, 08006907BB7D, 08006902E7CF, 0800690C1DF2, 0800690C9B7B, 08006905E63C, 0800690A0BA5, 08006909D93B, 080069097A4D, 080069097A4E, 0800690C9AA2, 0800690AC0A3, 0800690ABEE0, 080069086F94, 0800690883CD, 080069088319, 0800690A8830, 0800690A8841, 080069090953, 0800690761D4, 0800690C229, 08006907BEE0, 080069076231, 08006907622F, 080069107342, 08006909D80B, 080069099D0A, 0800690ED67D, 08006910560F, 080069105607, 080069106136, 080069088273, 080069A14138, 08006907BEB2, 0800690A8F6D, 0800690A8F4F, 0800690EAF6D, 0800690EB40C, 08006907BB6D, 0800690C1E69, 08006905A8E6, 08006905A225, 08006908A3A8, 0800690A02FD, 0800690A854C, 0800690A4677, 0800690A37AE, 08006905C04D, 08006909FD0C, 08006909FD1B, 0800690A4670, 08006906D9B0, 08006906D94E, 080069087078, 0800690883D0, 0800690977C2, 08006909D8DE, 08006909D8DA, 08006908706A, 08006909F1BB, 0800690A9B6B, 0800690A466D, 08006909DA0F, 0800690A4565, 080069100F06, 080069103003, 08869103015, 080069103265, 08006910326F, 08006902E7F8, 0800690E7279, 08006902E7F0, 0800690A0FE4, 08006909F507, 0800690EA365, 0800690C6356, 08006907BB7E, 0800690EA40C, 080069085E1, 080069102A57, 0800690EC864, 080069.0EAFCF, 08006910001E, 08006910623A, 08006910624F, 08006907B051, 08006910178B, 0800690EBC3A, 0800690EBBFF, 0800690EBFCA, 0800690A2507, 0800690E9A67, 0800690909AB, 08006902E925, 0800691050AF, 0800690ABF4D, 0800690A0FE1, 0800690AB4C1, 0800690AC55A, 0800690A2865, 0800690A25BA, 0800690AB1EE, 0800690C2168, 0800690A85FB, 0800690949E1, 080069106B53, 08006910816B, 0800690A73DA, 08006908EFB4, 080069090A10, 0800690C2B4E, 0800690883C8, 08006909673B, 0800690A0FE5, 08006905BE74, 080069087023, 0800690E82C4, 080069088463, 08006909EFA6, 080069099D13, 0800690EACE8, 08006908847A, 0800690EADC5, 0800691050D5, 0800690A97D1, 088690A1DC6, 0800690BD8A4, 080069134331, 0800691048A5, 0800690F6E74, 0800690841C6, 08800690C21B1, 0800690A9D0E, 0800690A87F2, 0800690CECEA, 0800690CDF04, 08700690761CF, 08006907DADE, 0800690CDDA2, 0800690E72F7, 0800690A02FC, 0800690A47CE, 0800690A47E5, 0800690A47AE, 08006902E8DB, 08006910762B, 08006910762A, 0800690CE165, 080069077BB7, 08006905EB6E, 080069087A27, 0800690E7283, 0800690937BB, 080069090260, 08006910621E
  • Product Classification
    Radiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA and the countries of Bulgaria, Switzerland, Czech Republic, Germany, Spain, France, Hungary, Ireland, Italy, Liechtenstein, Netherlands, Poland, Portugal, Sweden, Slovak Republic, Australia, China, Hong Kong, and Japan,
  • Product Description
    PrecisePLAN Treatment Planning System || To plan multiple beam radiation therapy treatments.
  • Manufacturer
    Elekta, Inc.

Manufacturer

Elekta, Inc.
  • Manufacturer Address
    Elekta, Inc., 4775 Peachtree Industrial Blvd, Bldg 300, #300, Norcross GA 30092-3011
  • Manufacturer Parent Company (2017)
    Elekta AB
  • Source
    USFDA