International safety notice
Safety Notice for the counterfeit product Juvederm Ultra 4, Pharm-Allergan GmbH
Germany / BfArM · DEU · Jan 13, 2015
Key facts
| Title | Safety Notice for the counterfeit product Juvederm Ultra 4, Pharm-Allergan GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the counterfeit product Juvederm Ultra 4, Pharm-Allergan GmbH |
| Manufacturer | Safety Notice for the counterfeit product Juvederm Ultra 4, Pharm-Allergan GmbH |
| Models | 500580, 53175, 12345, 92038-10, „2016, 920381-0, S30LA30262, D-60327, 4-PRODUKTEN, 43585986, 920381-100, „2014.04 |
| Date | Jan 13, 2015 |
| 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