International safety notice
Recall of the product AMO TECNIS iTec Preloaded Delivery System, Abbott Medical Optics Inc.
Germany / BfArM · DEU · Feb 7, 2014
Key facts
| Title | Recall of the product AMO TECNIS iTec Preloaded Delivery System, Abbott Medical Optics Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the product AMO TECNIS iTec Preloaded Delivery System, Abbott Medical Optics Inc. |
| Manufacturer | Recall of the product AMO TECNIS iTec Preloaded Delivery System, Abbott Medical Optics Inc. |
| Models | 5527721306, 5527481306, 5528351306, 5528281306, 5528451306, 5527341306, 5527981306, 5528381306, 5528121306, 5528311306, 5527901306, 5527991306 and 103 more |
| Date | Feb 7, 2014 |
| 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