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Terminated

VeriCal Calibrator Set

FDA Recall Z-0032-06 · Posted 2005-10-22

Recalling FirmBIOMERIEUX, INC.
Recall StatusTerminated
Product CodeJPA
Date Initiated2005-08-19
Date Terminated2006-10-16
Product Quantity2334 kits

Reason for Recall

The product is being recalled due to mis-assignment of ISI values associated with VeriCal use.

Firm Action

Consignees were notified on/about 08/31/2005.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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