International safety notice
Recall for Endoloop Ligature PDS II Suture, Johnson & Johnson
Germany / BfArM · DEU · Jul 10, 2009
Key facts
| Title | Recall for Endoloop Ligature PDS II Suture, Johnson & Johnson |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Endoloop Ligature PDS II Suture, Johnson & Johnson |
| Manufacturer | Recall for Endoloop Ligature PDS II Suture, Johnson & Johnson |
| Models | 2093103, BAX225 |
| Date | Jul 10, 2009 |
| 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