ClearanceBrief
Recall Z-1931-2012 ยท NBC Test, Natriuretic Peptide

Alere San Diego, Inc.

Alere Triage BNP PN 98000XR Intended to be used as an aid in the diagnosis and assessment of severity of congestive heart failure (also referred to as heart failure).

DateJul 6, 2012 (initiated May 22, 2012)
StatusTerminated
ReasonCertain lots of the affected products may have significantly decreased precision relative to the package insert, which could result in an increased frequency of false positive or false negative results. These false positive and false negative results are unpredictable within lots and may not be detected by Quality Control testing.
Root causeProcess design
ActionPhase 1 of the recall included a recall communication being initiated on May 22, 2012 with Alere forwarding a recall letter to all their customers who purchased the Triage CardioProfiler Panel, Triage Cardiac Panel, Triage Profiler SOB Panel, Triage BNP, and Triage D-dimer. The letter informed the customers of the problems identified and the actions to be taken. Customers were instructed to discontinue use of the affected product, and to complete and fax the enclosed verification form within 10 days. Phase 2 of the recall included a recall communication letter being forwarded to custome
Quantity30,083 kits
DistributionNationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K051781GRAFTCAGE TLX
Osteotech, Inc., Dec 16, 2005