International safety notice
Lot Recall for the Passeo-18 balloon catheter, Biotronik
Germany / BfArM · DEU · May 26, 2011
Key facts
| Title | Lot Recall for the Passeo-18 balloon catheter, Biotronik |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Passeo-18 balloon catheter, Biotronik |
| Manufacturer | Lot Recall for the Passeo-18 balloon catheter, Biotronik |
| Models | 01100398, 01100674, 01100181, 01101193, CH-8180, 01102252, 1208XXXX, 0909XXXX, 0409XXXX, 01100399, 01100397, 0608XXXX and 41 more |
| Date | May 26, 2011 |
| 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