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U.S. Department of Health and Human Services

Class 2 Device Recall Uroglogix Targis

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 Class 2 Device Recall Uroglogix Targissee related information
Date Initiated by FirmMarch 16, 2007
Date PostedApril 05, 2007
Recall Status1 Terminated 3 on May 25, 2007
Recall NumberZ-0721-2007
Recall Event ID 37638
PMA NumberP970008 
Product Classification Microwave Delivery System - Product Code MEQ
ProductUrologix Microwave Delivery System 2.5 - 3.5 For use with prostatic urethra lengths of 2.5-3.5 cm only. Model TA1321D.
Code Information Individual catheter lot number KG001346 for model TA1321D. Kit box lot number KGP111105.
Recalling Firm/
Manufacturer		 Urologix, Inc.
14405 21st Ave N
Minneapolis MN 55447-4685
Manufacturer Reason
for Recall		The catheter in the kit matches the description on the kit and pouch label; however, an incorrect label was placed onto the catheter during manufacturing.
FDA Determined
Cause 2		Other
ActionA letter dated 3/16/07 was FedEx overnight to consignees. The letter described the product, problem and gave instructions for returning and replacing the affected product.
Quantity in Commerce21
DistributionNationwide and the Netherlands.
Total Product Life CycleTPLC Device Report
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.
PMA DatabasePMAs with Product Code = MEQ
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