BEUDAMED
    FDA Recall Terminated

    MedRo Rx -Reverse Osmosis System All Models All Voltages, All Voltages

    Recall: Z-0798-05 · Initiated February 28, 2005

    Recall

    Recall Number
    Z-0798-05
    Event Number
    31255
    Firm
    U.S. Filter/Ionpure, Inc.
    FEI Number
    1000121072
    Product Code
    FIP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    February 28, 2005
    Posted
    May 6, 2005
    Terminated
    May 15, 2012
    Address
    10 Technology Dr, Lowell, MA, 01851-2728

    Description

    MedRo Rx -Reverse Osmosis System All Models All Voltages, All Voltages

    Reason

    Incorrect type of stainless steel firm used 303 vs 316

    Action

    US Filter notified consignees by letter between 3/17 and 3/28/05 advising users of the recall.US Service will field correct and replace units.

    Distribution

    Nationwide Foreign: Canada, Mexico

    Quantity

    282 units