International safety notice
Lot Recall for Turbo-Booster Laser Guide Catheters, Spectranetics
Germany / BfArM · DEU · Jul 27, 2011
Key facts
| Title | Lot Recall for Turbo-Booster Laser Guide Catheters, Spectranetics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Turbo-Booster Laser Guide Catheters, Spectranetics |
| Manufacturer | Lot Recall for Turbo-Booster Laser Guide Catheters, Spectranetics |
| Date | Jul 27, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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