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U.S. Department of Health and Human Services

Class 3 Device Recall

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 Class 3 Device Recallsee related information
Date Initiated by FirmMay 13, 2004
Date PostedMarch 23, 2005
Recall Status1 Terminated 3 on August 31, 2009
Recall NumberZ-0648-05
Recall Event ID 31009
Product Classification Collector, Urine, (And Accessories) For Indwelling Catheter - Product Code KNX
ProductLatex Free*** REF B1000P Belly Bag Urine Collection Bag with Sample Port***1000 ml LOT***Sterile EO*** Single use only, Manufactured and Distributed by***Rusch Inc., 245 Meadowbrook Parkway, Duluth, GA 30096***Quantity 10****
Code Information Lots 121848, 122514, 124332, 125309 and 125885
FEI Number 2429473
Recalling Firm/
Manufacturer		 Teleflex Medical, Inc.
2450 Meadowbrook Pkwy
Duluth GA 30096-4635
For Additional Information ContactMs Diane Luo
919-361-4034
Manufacturer Reason
for Recall		Firm received complaints of leaking urine collection bags.
FDA Determined
Cause 2		Other
ActionConsignees were notified by letter on 5/13/2004. A follow up letter was sent on 11/22/2004.
Quantity in Commerce1227 bags
DistributionNationwide, Australia, Japan and the UK
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.
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