International safety notice
Recall of the PI-128 Intraducer Peritoneal Catheter from TAUT
Germany / BfArM · DEU · Mar 7, 2007
Key facts
| Title | Recall of the PI-128 Intraducer Peritoneal Catheter from TAUT |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the PI-128 Intraducer Peritoneal Catheter from TAUT |
| Manufacturer | Recall of the PI-128 Intraducer Peritoneal Catheter from TAUT |
| Models | 232-2507, KC05107, KC06025, 05178, KC06060, PT-128, 232-8005, KC06002, 04116, PI-128, 50000, KC06116 and 3 more |
| Date | Mar 7, 2007 |
| 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