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
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