Access Immunoassay Systems CORTISOL, Part Number: 33600
FDA Recall Z-2621-2010 · Posted 2010-09-29
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Recalling FirmBeckman Coulter Inc.
Recall StatusTerminated
Product CodeCGR
Date Initiated2010-02-17
Date Terminated2012-04-19
Product Quantity7282 units
Reason for Recall
The recall was initiated by Beckman Coulter after the firm confirmed customer reports that the affected lot of Access Cortisol reagent (REF 33600) identified above may produce suppressed patient results. Beckman Coulter also confirmed customer reports that the two lots of Access Progesterone reagent (REF 33550) identified above may produce suppressed patient results and an increased incidence of I
Firm Action
Two (2) Product Corrective Action (PCA) letters with attached Customer Response form were sent on the week of February 15, 2010 to the affected customers. The letters provide the customers with an explanation of the problem identified and instruct the customers to discontinue use of Access Progesterone and Access Cortisol Reagents, lot numbers referenced.
For product replacements consignees were instructed :
(1) In the United States, please contact Customer Service at 1-800-526-3821;
(2) In Canada, please contact Customer Service at 1-800-463-7828;
(3) Outside of the United States and Canada, contact your local Beckman Coulter Representative.
If consignees 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. Outside the United States and Canada, contact your local Beckman Coulter Representative.
Root Cause
Other
Distribution Pattern
United States & 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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