International safety notice
Lot Recall of VORTEK® Double Loop Ureteral Stent Open/Open With Connectable Pusher and VORTEK® Hydro-Coated Double Loop Ureteral Stents, Coloplast
Germany / BfArM · DEU · Nov 25, 2013
Key facts
| Title | Lot Recall of VORTEK® Double Loop Ureteral Stent Open/Open With Connectable Pusher and VORTEK® Hydro-Coated Double Loop Ureteral Stents, Coloplast |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot Recall of VORTEK® Double Loop Ureteral Stent Open/Open With Connectable Pusher and VORTEK® Hydro-Coated Double Loop Ureteral Stents, Coloplast |
| Manufacturer | Lot Recall of VORTEK® Double Loop Ureteral Stent Open/Open With Connectable Pusher and VORTEK® Hydro-Coated Double Loop Ureteral Stents, Coloplast |
| Models | ACB1B11002, 3730556, 3699744, BCFA541002, 21035, 69749917, 3692086, 3699728, 3700388, ACB1B21002, 3730549, 3709109 and 48 more |
| Date | Nov 25, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1