International safety notice
Recall for LENTIS HydroSmart foldable Intraocular lenses in glass vials, Oculentis GmbH
Germany / BfArM · DEU · Dec 8, 2014
Key facts
| Title | Recall for LENTIS HydroSmart foldable Intraocular lenses in glass vials, Oculentis GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | LENTIS HydroSmart foldable Intraocular lenses in glass vials, Oculentis GmbH |
| Manufacturer | Recall for LENTIS HydroSmart foldable Intraocular lenses in glass vials, Oculentis GmbH |
| Models | 430955-11, 430955-0, DE174093520, L-402, 2014-12-04, 2014-001, 3-PIECE, 73515, 20000, CE1275, 13507, 0.011 |
| Date | Dec 8, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 10–99 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