International safety notice
Recall for the product BVI CustomEyes® Ophthalmic Procedure Kits, Beaver-Visitec International Sales Ltd.
Germany / BfArM · DEU · Jun 15, 2015
Key facts
| Title | Recall for the product BVI CustomEyes® Ophthalmic Procedure Kits, Beaver-Visitec International Sales Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product BVI CustomEyes® Ophthalmic Procedure Kits, Beaver-Visitec International Sales Ltd. |
| Manufacturer | Recall for the product BVI CustomEyes® Ophthalmic Procedure Kits, Beaver-Visitec International Sales Ltd. |
| Date | Jun 15, 2015 |
| 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