BEUDAMED
    FDA Recall Terminated

    Microcuff Adult Endotracheal Tubes - Oral/Nasal Magill with Murphy Eye * ID Size: 5,0mm, Microcuff Product Reference: I-HMICU-50; ID Size: 5.5mm, Product Reference: I-HMICU- 55; ID Size: 6.0mm, Product Reference: I-HMICU- 60; ID Size: 6.5mm, Product Reference: I-HMICU- 65; ID Size: 7.0mm, Product Reference: I-HMICU- 70; ID Size: 7.5mm, Product Reference: I-HMICU-75; ID Size: 8.0mm, Product Reference: I-HMICU-80; ID Size: 8.5mm, Product Reference: I-HMICU-85; ID Size: 9.0mm, Product Reference: I-HMICU-90; and ID Size: 10.0mm Product Reference: I-HMICU-10 * Sterile * Single use only * Manufactured by Euromedical Industries, Sdn. Bhd., Bakar Arang Industrial Estate, 08000 Sungai Patani, Kedah, Malaysia * Distributed by: Microcuff GmbH, Hohnerweg 2-4, D-69469 Weinheim, Germany.

    Recall: Z-1265-06 · Initiated June 19, 2006

    Recall

    Recall Number
    Z-1265-06
    Event Number
    35753
    Firm
    Microcuff Gmbh Honer
    FEI Number
    3005301443
    Product Code
    BTR
    Status
    Terminated
    Root Cause
    Other
    Initiated
    June 19, 2006
    Posted
    July 25, 2006
    Terminated
    May 1, 2007
    Address
    Weg 2 4, Weinheim, Germany

    Description

    Microcuff Adult Endotracheal Tubes - Oral/Nasal Magill with Murphy Eye * ID Size: 5,0mm, Microcuff Product Reference: I-HMICU-50; ID Size: 5.5mm, Product Reference: I-HMICU- 55; ID Size: 6.0mm, Product Reference: I-HMICU- 60; ID Size: 6.5mm, Product Reference: I-HMICU- 65; ID Size: 7.0mm, Product Reference: I-HMICU- 70; ID Size: 7.5mm, Product Reference: I-HMICU-75; ID Size: 8.0mm, Product Reference: I-HMICU-80; ID Size: 8.5mm, Product Reference: I-HMICU-85; ID Size: 9.0mm, Product Reference: I-HMICU-90; and ID Size: 10.0mm Product Reference: I-HMICU-10 * Sterile * Single use only * Manufactured by Euromedical Industries, Sdn. Bhd., Bakar Arang Industrial Estate, 08000 Sungai Patani, Kedah, Malaysia * Distributed by: Microcuff GmbH, Hohnerweg 2-4, D-69469 Weinheim, Germany.

    Reason

    Inadequate seals and/or holes in the pouch may compromise the sterility of the product.

    Action

    A notification by telephone was made in April 2006. A confirmation letter was later sent on 6/29/2006.

    Distribution

    U.S.

    Quantity

    1730 units (total for all three types)