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U.S. Department of Health and Human Services

Class 2 Device Recall INTELECT VET

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 Class 2 Device Recall INTELECT VETsee related information
Date Initiated by FirmDecember 17, 2007
Date PostedJune 25, 2008
Recall Status1 Terminated 3 on February 19, 2010
Recall NumberZ-1223-2008
Recall Event ID 46281
510(K)NumberK031077 
Product Classification Canine and equinine Muscle stimulator and therapeutic ultrasound - Product Code MPH
ProductINTELECT VET, Model No. 2756, Chattanooga Group, Hixson, TN 37343, Made in the USA
Code Information Serial numbers 1000 - 1140
Recalling Firm/
Manufacturer		 Chattanooga Corp Inc
4717 Adams Rd
Hixson TN 37343
For Additional Information ContactMr. Ben Whalen
423-648-4945
Manufacturer Reason
for Recall		Device malfunction: causing electric shock and burn.
FDA Determined
Cause 2		Device Design
ActionBeginning 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.
Quantity in Commerce140 units
DistributionWorldwide Distribution - including USA
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = MPH
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