International safety notice
Lot recall of AcrySof IQ IOL with UltraSert Implantation System, Alcon Pharma GmbH
Germany / BfArM · DEU · Jul 28, 2016
Key facts
| Title | Lot recall of AcrySof IQ IOL with UltraSert Implantation System, Alcon Pharma GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of AcrySof IQ IOL with UltraSert Implantation System, Alcon Pharma GmbH |
| Manufacturer | Lot recall of AcrySof IQ IOL with UltraSert Implantation System, Alcon Pharma GmbH |
| Models | 12409026, SN60WF, AU00T0.195, 12409013, AU00T0.220, 99338, 12409024, 12407087, 12407022, 12409028, 1304-99338, AU00T0.175 and 2 more |
| Date | Jul 28, 2016 |
| 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