International safety notice
Urgent Safety Notice for the product VarioFit® (cemented), aap Implantate AG
Germany / BfArM · DEU · Oct 20, 2014
Key facts
| Title | Urgent Safety Notice for the product VarioFit® (cemented), aap Implantate AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product VarioFit® (cemented), aap Implantate AG |
| Manufacturer | Urgent Safety Notice for the product VarioFit® (cemented), aap Implantate AG |
| Models | 49-30-75019-111, 2014-01, 350500, 0010-02, 64083, 0015-02, 2015-02, 0010-01, 0013-02, 2012-02, 0014-02, 5019-0 and 22 more |
| Date | Oct 20, 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