International safety notice
Recall of the peritoneal dialysis patient connectors PD Night Vario Plus Set, PD Night Vario Plus Paed Set and PD-Paed System from Fresenius
Germany / BfArM · DEU · Jul 12, 2007
Key facts
| Title | Recall of the peritoneal dialysis patient connectors PD Night Vario Plus Set, PD Night Vario Plus Paed Set and PD-Paed System from Fresenius |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the peritoneal dialysis patient connectors PD Night Vario Plus Set, PD Night Vario Plus Paed Set and PD-Paed System from Fresenius |
| Manufacturer | Recall of the peritoneal dialysis patient connectors PD Night Vario Plus Set, PD Night Vario Plus Paed Set and PD-Paed System from Fresenius |
| Models | OAS022, OBS221, OAS021, OAS281, OBS222, NMS012, OBS0811, OCS201, NMS013, NLS242, OCS211, OAS024 and 10 more |
| Date | Jul 12, 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