Atlas FDA

Latex Free*** REF B1000P Belly Bag Urine Collection Bag with Sample Port***1000 ml LOT***Sterile EO*** Single use only,

FDA device recall Z-0648-05 · posted 2005-03-23 · Terminated

Recall details

Recalling firm
Teleflex Medical, Inc.
Reason for recall
Firm received complaints of leaking urine collection bags.
Action taken
Consignees were notified by letter on 5/13/2004. A follow up letter was sent on 11/22/2004.
Root cause
Other
Status
Terminated
Product code
KNX
Quantity affected
1227 bags
Distribution
Nationwide, Australia, Japan and the UK
Date initiated
2004-05-13
Date posted
2005-03-23
Date terminated
2009-08-31
Location
Duluth, GA

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.