BEUDAMED
    FDA Recall Terminated

    Y-valve and T-valve, PSD/4 Syringe Drive Module parts.

    Recall: Z-0087-06 · Initiated August 24, 2005

    Recall

    Recall Number
    Z-0087-06
    Event Number
    33435
    Firm
    Hamilton Co
    FEI Number
    2915796
    Product Code
    JJC
    Status
    Terminated
    Root Cause
    Other
    Initiated
    August 24, 2005
    Posted
    October 22, 2005
    Terminated
    March 24, 2006
    Address
    4970 Energy Way, Reno, NV, 89502-4123

    Description

    Y-valve and T-valve, PSD/4 Syringe Drive Module parts.

    Reason

    The product valve has a high probability of deforming and may result in leakage during use.

    Action

    Recall initiated on 08/24/2005. The firm issued notification to its consignees via overnight letter, and via e-mail for its distributor (Hamilton Bonaduz).

    Distribution

    One distributor and 8 consumers received this product in CA, MA, MI, WI, Japan and Switzerland.

    Quantity

    271 Y and 78 T valves were distributed.