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Terminated

INTELECT ADVANCED, Model No. 2772MC, Chattanooga Group, Hixson, TN 37343, Made in the USA, Not for sale in the U.S.A.

FDA Recall Z-1229-2008 · Posted 2008-06-25

Recalling FirmChattanooga Corp Inc
Recall StatusTerminated
Product CodeMPH
Date Initiated2007-12-17
Date Terminated2010-02-19
Product Quantity2002 units

Reason for Recall

Device malfunction: causing electric shock and burn.

Firm Action

Beginning on 12/17/2007, Chattanooga Corp. sent two recall notification letters, via UPS mail, to its consignees informing them of the situation. The letters stated that the recall was to the user level and requested that the user perform the software upgrade, which will eliminate the possibility of shock and burn.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution - including USA

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K031077VECTRA EPR SYSTEM AND INTELECT EPR SYSTEMChattanooga Group · 2003-12-11

Official Source

View FDA Recall →

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

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