International safety notice
Recall and after-care recommendation for WATCHMAN FLX Left Atrial Appendage (LAAC) Closure Device, Boston Scientific International S.A.
Germany / BfArM · DEU · Oct 7, 2016
Key facts
| Title | Recall and after-care recommendation for WATCHMAN FLX Left Atrial Appendage (LAAC) Closure Device, Boston Scientific International S.A. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | WATCHMAN FLX Left Atrial Appendage (LAAC) Closure Device, Boston Scientific International S.A. |
| Manufacturer | Recall and after-care recommendation for WATCHMAN FLX Left Atrial Appendage (LAAC) Closure Device, Boston Scientific International S.A. |
| Models | 18944587, 18876066, 18838165, 18409435, 18408202, 93420, 18396811, 18707086, 18682283, WS5020, 18900178, 18435077 and 116 more |
| Date | Oct 7, 2016 |
| 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