International safety notice
Recall of certain lots of two products (Pipeline Embolization Device and Alligator Retrieval Device), COVIDIEN
Germany / BfArM · DEU · Apr 17, 2014
Key facts
| Title | Recall of certain lots of two products (Pipeline Embolization Device and Alligator Retrieval Device), COVIDIEN |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of certain lots of two products (Pipeline Embolization Device and Alligator Retrieval Device), COVIDIEN |
| Manufacturer | Recall of certain lots of two products (Pipeline Embolization Device and Alligator Retrieval Device), COVIDIEN |
| Date | Apr 17, 2014 |
| 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