International safety notice
Recall of Endopath®Probe Plus II Electrosurgical Suction Irrigation Products from Ethicon
Germany / BfArM · DEU · Jun 14, 2006
Key facts
| Title | Recall of Endopath®Probe Plus II Electrosurgical Suction Irrigation Products from Ethicon |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Endopath®Probe Plus II Electrosurgical Suction Irrigation Products from Ethicon |
| Manufacturer | Recall of Endopath®Probe Plus II Electrosurgical Suction Irrigation Products from Ethicon |
| Models | EPS11, EPS08, EPS06, EPS03, EPH02, EPS01, EPS13, EPS04, EPH04, EPS02, PROBEPLUSII-2006-04-21, EPH01 and 1 more |
| Date | Jun 14, 2006 |
| 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