Access Immunoassay Systems AFP QC, Part Number: 33219 The Access AFP QC is intended for monitoring system performance of immunoenzymatic procedures for the quantitative measurement of alpha-fetoprotein (AFP) using the Access Immunoassay Systems.
FDA Recall Z-2208-2010 · Posted 2010-08-11
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Recalling FirmBeckman Coulter Inc.
Recall StatusTerminated
Product CodeJJX
Date Initiated2010-04-21
Date Terminated2012-05-07
Product Quantity166
Reason for Recall
The recall was initiated after Beckman Coulter confirmed an issue with the Access AFP QC kits (REF 33219) which contain three levels of control material identified as QC1, QC2, and QC3, Beckman Coulter has confirmed that vials of QC1 in the kit lots identified above contain microbial contamination. Customers may see that the results from a contaminated vial of QC1 are within the established refere
Firm Action
A Product Corrective Action (PCA) letter was sent
on the week of April 19, 2010 to all customers who
purchased the Access Immunoassay Systems AFP
QC material, lot numbers referenced above. The
letter provided the customers with an explanation of
the problem identified and instructed the customers
to (1) Please discard all remaining inventory of the three Access AFP QC kit lots identified above,
including all vials of QC1, QC2, and QC3.
(2) Please review your ac and patient results obtained while using the affected control lots. Interpret Access AFP test results in light of the clinical presentation of the patient, including: symptoms,
clinical history, data from other tests and other appropriate information.
(3) Please share this information with your laboratory staff and retain this notification as part of your
laboratory Quality System documentation.
(4) Complete and return the enclosed response form
within 10 days so we can be assured that you have received this important notification.
For customers that need assistance or have any questions regarding this notification, they were instructed to contact Technical Support at 1-800-854-3633 in the United States and Canada.
Root Cause
Other
Distribution Pattern
Nationwide and Canada
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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