BEUDAMED
    FDA Recall Terminated

    Portable Oxygen Generator

    Recall: Z-1368-05 · Initiated August 1, 2005

    Recall

    Recall Number
    Z-1368-05
    Event Number
    32735
    Firm
    Inogen, Inc
    FEI Number
    3004672275
    Product Code
    CAW
    Status
    Terminated
    Root Cause
    Other
    Initiated
    August 1, 2005
    Posted
    August 12, 2005
    Terminated
    February 13, 2007
    Address
    120 Cremona Dr, Ste B, Goleta, CA, 93117-5564

    Description

    Portable Oxygen Generator

    Reason

    Firm plans to upgrade all units to correct situations that could lead to interuption in oxygen delivery.

    Action

    Recall is scheduled to begin August 1st 2005 by letter to customers informing them that the units will be upgraded on a predetermined schedule. Firm estimates completion in 6 months.

    Distribution

    Nationwide

    Quantity

    900