BEUDAMED
    FDA Recall Terminated

    50 mL sterile plastic centerfuge tubes.

    Recall: Z-0512-04 · Initiated December 29, 2003

    Recall

    Recall Number
    Z-0512-04
    Event Number
    28016
    Firm
    Stockwell Scientific Inc
    FEI Number
    3000013175
    Product Code
    JKA
    Status
    Terminated
    Root Cause
    Other
    Initiated
    December 29, 2003
    Posted
    February 4, 2004
    Terminated
    April 8, 2004
    Address
    7325 E Evans Rd, Scottsdale, AZ, 85260-3101

    Description

    50 mL sterile plastic centerfuge tubes.

    Reason

    Tubes are brittle and break during centerfuging specimens.

    Action

    Firm sent a recall letter to all customers 12/30/2003 requesting return of existing stock and subrecall of subdistributed product.

    Distribution

    Nationwide and Canada

    Quantity

    3762 cases (500 tubes/cs)