International safety notice
Lot / batch recall of Turbo Elite atherectomy catheter / ELCA coronary atherectomy catheter, Spectranetics Corporation
Germany / BfArM · DEU · Nov 22, 2016
Key facts
| Title | Lot / batch recall of Turbo Elite atherectomy catheter / ELCA coronary atherectomy catheter, Spectranetics Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot / batch recall of Turbo Elite atherectomy catheter / ELCA coronary atherectomy catheter, Spectranetics Corporation |
| Manufacturer | Lot / batch recall of Turbo Elite atherectomy catheter / ELCA coronary atherectomy catheter, Spectranetics Corporation |
| Models | CVX-300®, 80921, 719.447.2469 |
| Date | Nov 22, 2016 |
| 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