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Terminated

Diasorin LIAISON (R) Chemiluminescence Analyzer Model # 15970. Colorimeter, Photometer, Spectrophotometer for clinical use.

FDA Recall Z-1042-2009 · Posted 2009-03-30

Recalling FirmDiasorin Inc.
Recall StatusTerminated
Product CodeJJQ
Date Initiated2008-12-05
Date Terminated2012-05-22
Product Quantity9

Reason for Recall

DiaSorin determined that there was a potential for a short to occur in a a residual starter pump electrical cable in the LIAISON (R) Analyzer.

Firm Action

DiaSorin Inc authorized Field Service Engineer has visited the sites and performed the necessary field correction. Upon completion of their work, the field service engineer generated a Field Service Report and a copy was left with the customer.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution -- USA including states of NC, NJ, PA, CA, WA, MO, UT, and OR and country of Canada.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K032844LIAISON 25 OH VITAMIN DDiaSorin, Inc. · 2004-02-12

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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