International safety notice
Recall Endopath ETS 35 mm, Johnson & Johnson
Germany / BfArM · DEU · May 21, 2008
Key facts
| Title | Recall Endopath ETS 35 mm, Johnson & Johnson |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall Endopath ETS 35 mm, Johnson & Johnson |
| Manufacturer | Recall Endopath ETS 35 mm, Johnson & Johnson |
| Models | D4H546, D4HXID, D4J91D, D4H052, D4HD96, D4H98J, D4HG9G, D4HN53, D4GPOJ, D4HT53, MRZ-2012, D4HG66 and 254 more |
| Date | May 21, 2008 |
| 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