BEUDAMED
    FDA Recall Terminated

    SSCOR Suction Device Model 2314

    Recall: Z-0414-05 · Initiated January 6, 2005

    Recall

    Recall Number
    Z-0414-05
    Event Number
    30845
    Firm
    S S C O R Inc
    FEI Number
    2022724
    Product Code
    BTA
    Status
    Terminated
    Root Cause
    Other
    Initiated
    January 6, 2005
    Posted
    January 27, 2005
    Terminated
    June 13, 2011
    Address
    11064 Randall St, Sun Valley, CA, 91352-2621

    Description

    SSCOR Suction Device Model 2314

    Reason

    Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.

    Action

    SSCOR Powered Suction Device not performing as intended.

    Distribution

    CA, FL, IA, IL, IN, KY, MO, NC, NJ, NY, OH, France, New Zealand, Singapore, United Kingdom

    Quantity

    378