International safety notice
Recall for the intraocular lens “SENSAR Foldable IOL with OptiEdge”, AMO
Germany / BfArM · DEU · Nov 21, 2011
Key facts
| Title | Recall for the intraocular lens “SENSAR Foldable IOL with OptiEdge”, AMO |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the intraocular lens “SENSAR Foldable IOL with OptiEdge”, AMO |
| Manufacturer | Recall for the intraocular lens “SENSAR Foldable IOL with OptiEdge”, AMO |
| Models | 5186021009, 5059311009, 5059601009, 5059511009, 5059791009, 5185721009, 5059501009, 5059011009, 5185961009, 5185851009, 5059651009, 5059081009 and 178 more |
| Date | Nov 21, 2011 |
| 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