International safety notice
Corrective action for Infusion pump CODAN ARGUS 71XV and Syringe pump CODAN ARGUS 606S, CODAN ARGUS AG
Germany / BfArM · DEU · Oct 14, 2014
Key facts
| Title | Corrective action for Infusion pump CODAN ARGUS 71XV and Syringe pump CODAN ARGUS 606S, CODAN ARGUS AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Infusion pump CODAN ARGUS 71XV and Syringe pump CODAN ARGUS 606S, CODAN ARGUS AG |
| Manufacturer | Corrective action for Infusion pump CODAN ARGUS 71XV and Syringe pump CODAN ARGUS 606S, CODAN ARGUS AG |
| Models | INFORMATION_3_2014, CH-6340, 18.261_A, A606S, A71XV |
| Date | Oct 14, 2014 |
| 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