International safety notice
Recall and updated instructions for use for Lifetech CeraFlex Atrial Septal Defect (ASD) Occluder, Lifetech Scientific (Shenzhen) Co. Ltd.
Germany / BfArM · DEU · Apr 1, 2016
Key facts
| Title | Recall and updated instructions for use for Lifetech CeraFlex Atrial Septal Defect (ASD) Occluder, Lifetech Scientific (Shenzhen) Co. Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lifetech CeraFlex Atrial Septal Defect (ASD) Occluder, Lifetech Scientific (Shenzhen) Co. Ltd. |
| Manufacturer | Recall and updated instructions for use for Lifetech CeraFlex Atrial Septal Defect (ASD) Occluder, Lifetech Scientific (Shenzhen) Co. Ltd. |
| Models | 141014112, 141015167, 141014106, 141014119, 141014157, 141015144, 141015136, 140921122, 140917148, 140916145, 141015180, 140916207 and 483 more |
| Date | Apr 1, 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