International safety notice
Recall for Wiseguide Guide Catheter, Boston Scientific
Germany / BfArM · DEU · Apr 15, 2009
Key facts
| Title | Recall for Wiseguide Guide Catheter, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Wiseguide Guide Catheter, Boston Scientific |
| Manufacturer | Recall for Wiseguide Guide Catheter, Boston Scientific |
| Models | 20122100, 20133545, 1950048, 19500-OS, 20121000, 20125185, 20115948, H749195002410, 20133576, 049198154720, 20133553, 2011169B and 2006 more |
| Date | Apr 15, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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