International safety notice
Lot Recall for the Ascendra2™ Transapical Delivery System, Edwards Lifesciences LLC
Germany / BfArM · DEU · Dec 2, 2011
Key facts
| Title | Lot Recall for the Ascendra2™ Transapical Delivery System, Edwards Lifesciences LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Ascendra2™ Transapical Delivery System, Edwards Lifesciences LLC |
| Manufacturer | Lot Recall for the Ascendra2™ Transapical Delivery System, Edwards Lifesciences LLC |
| Models | 58926070, 59080387, 58906005, 58926072, 9320AS26, 9320AS23, 58927597, 58918804, 58927595, 58918803, 58915381, 58931231 and 26 more |
| Date | Dec 2, 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