The Alere Cholestech LDX high sensitivity C-Reactive Protein (hsCRP) Test Cassette, Model Number 12-807. Product Usage: Immunoassay for the determination of C-Reactive Protein (CRP). The Alere Cholestech LDX high sensitivity C-Reactive Protein (hsCRP) is an in vitro diagnostic test for the quantitative determination of C-reactive protein in whole blood or serum.
FDA Recall Z-1178-2013 · Posted 2013-04-25
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Recalling FirmAlere San Diego, Inc.
Recall StatusTerminated
Product CodeDCK
Date Initiated2013-03-06
Date Terminated2014-03-12
Product Quantity2333 kits
Reason for Recall
The Alere Cholestech LDX hsCRP
cassette (PN 12-807) may have increased imprecision relative to the performance data in the package insert,
which may cause differences in quantitative results for hsCRP compared to a reference method or
repeat testing on the same patient sample.
Firm Action
Alere sent an Urgent Medical Device Recall letter dated March 6, 2013 to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to block all stock of the affected lot in their warehouses; discontinue use and discard all stock on hand, complete the provided Customer Verification form to document disposal, contact their primary consignees and advise them of the required discontinuation and disposal of the affected lot. For question call 877-308-8289.
Root Cause
Nonconforming Material/Component
Distribution Pattern
USA Nationwide Distribution
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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