The Inlay Optima Ureteral Stent Without Guidewire Kit, 30 cm length, 6 Fr (C.R. Bard, model/catalogue 788630, lot NGJU4327) is affected. It was recalled because the pouch label may not match the actual product inside the packaging; contact the manufacturer for additional information.
What's being recalled
Companies: C.R. Bard, Inc., 8195 Industrial Blvd., Covington, Georgia, United States, 30014.
How to identify it
Affected products: Inlay Optima™ Ureteral Stent Without Guidewire Kit, Length 30cm, 6Fr; Lot or serial number: NGJU4327; Model or catalogue number: 788630
The hazard
BD has identified a labeling discrepancy involving Inlay Optima™ ureteral stents based on customer complaints. Our investigation has determined that the pouch label may not match the actual product within the packaging.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)