International safety notice
Recall for the port cannula Ambix NONCOR®stick Safe, Fresenius Kabi Deutschland AG
Germany / BfArM · DEU · Nov 7, 2014
Key facts
| Title | Recall for the port cannula Ambix NONCOR®stick Safe, Fresenius Kabi Deutschland AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the port cannula Ambix NONCOR®stick Safe, Fresenius Kabi Deutschland AG |
| Manufacturer | Recall for the port cannula Ambix NONCOR®stick Safe, Fresenius Kabi Deutschland AG |
| Models | 8081242, 32251284, 32193334, 8081272, 32245284, 32113514, 32362303, 32155354, 8084312, 09-OCT-2014, 8084232, 32354243 and 54 more |
| Date | Nov 7, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
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